结合性丙二酸及甲基丙二酸血症 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "结合性丙二酸及甲基丙二酸血症" in Chinese language version.

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Tucci, Sara. Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria. Orphanet Journal of Rare Diseases. 2020-12, 15 (1) [2024-09-03]. ISSN 1750-1172. PMC 6977288 . PMID 31969167. doi:10.1186/s13023-020-1299-7. （原始内容存档于2023-03-21）（英语）.

bmj.com

jmg.bmj.com

Alfares, A.; Nunez, L. D.; Al-Thihli, K.; Mitchell, J.; Melancon, S.; Anastasio, N.; Ha, K. C. H.; Majewski, J.; Rosenblatt, D. S.; Braverman, N. Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype. Journal of Medical Genetics. 2011-09-01, 48 (9) [2022-08-06]. ISSN 0022-2593. doi:10.1136/jmedgenet-2011-100230. （原始内容存档于2022-06-15）（英语）.

doi.org

de Sain-van der Velden, Monique G. M.; van der Ham, Maria; Jans, Judith J.; Visser, Gepke; Prinsen, Hubertus C. M. T.; Verhoeven-Duif, Nanda M.; van Gassen, Koen L. I.; van Hasselt, Peter M. A New Approach for Fast Metabolic Diagnostics in CMAMMA. Morava, Eva (编). JIMD Reports, Volume 30 30. Berlin, Heidelberg: Springer Berlin Heidelberg. 2016: 15–22 [2022-07-31]. ISBN 978-3-662-53680-3. PMC 5110436 . PMID 26915364. doi:10.1007/8904_2016_531. （原始内容存档于2022-09-22）.
Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A.; Brunel‐Guitton, Catherine; Braverman, Nancy E. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. 2019, 42 (1): 107–116 [2022-08-06]. ISSN 0141-8955. PMID 30740739. S2CID 73436689. doi:10.1002/jimd.12032. （原始内容存档于2022-09-22）（英语）.
Wehbe, Zeinab; Behringer, Sidney; Alatibi, Khaled; Watkins, David; Rosenblatt, David; Spiekerkoetter, Ute; Tucci, Sara. The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 2019-11, 1864 (11) [2022-08-06]. doi:10.1016/j.bbalip.2019.07.012. （原始内容存档于2022-06-19）（英语）.
NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R; O'Brien, Kevin; Hauser, Natalie S. Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. Nature Genetics. 2011-09, 43 (9) [2022-07-31]. ISSN 1061-4036. PMC 3163731 . PMID 21841779. doi:10.1038/ng.908. （原始内容存档于2022-09-21）（英语）.
Sniderman, Lisa C.; Lambert, Marie; Giguère, Robert; Auray-Blais, Christiane; Lemieux, Bernard; Laframboise, Rachel; Rosenblatt, David S.; Treacy, Eileen P. Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program. The Journal of Pediatrics. 1999-06, 134 (6) [2022-07-31]. doi:10.1016/S0022-3476(99)70280-5. （原始内容存档于2018-06-11）（英语）.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan. Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients. Frontiers in Pediatrics. 2021-11-25, 9 [2022-08-06]. ISSN 2296-2360. PMC 8658908 . PMID 34900860. doi:10.3389/fped.2021.751895. （原始内容存档于2022-09-21）.
Alfares, A.; Nunez, L. D.; Al-Thihli, K.; Mitchell, J.; Melancon, S.; Anastasio, N.; Ha, K. C. H.; Majewski, J.; Rosenblatt, D. S.; Braverman, N. Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype. Journal of Medical Genetics. 2011-09-01, 48 (9) [2022-08-06]. ISSN 0022-2593. doi:10.1136/jmedgenet-2011-100230. （原始内容存档于2022-06-15）（英语）.
Gregg, A. R.; Warman, A. W.; Thorburn, D. R.; O'Brien, W. E. Combined malonic and methylmalonic aciduria with normal malonyl-coenzyme A decarboxylase activity: A case supporting multiple aetiologies. Journal of Inherited Metabolic Disease. 1998, 21 (4): 382–390 [2022-08-06]. PMID 9700595. S2CID 20212973. doi:10.1023/A:1005302607897. （原始内容存档于2022-06-15）（英语）.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart. Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis. Journal of Biological Chemistry. 2011-09, 286 (39) [2022-07-31]. PMC 3190830 . PMID 21846720. doi:10.1074/jbc.M111.291591. （原始内容存档于2022-08-02）（英语）.
Lee, Joon Kee; Oh, Arum. Combined Malonic and Methylmalonic Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report. Journal of Korean Medical Science. 2023, 38 (45) [2024-09-01]. ISSN 1011-8934. PMC 10659923 . PMID 37987109. doi:10.3346/jkms.2023.38.e387. （原始内容存档于2024-06-30）（英语）.
Bowman, Caitlyn E.; Wolfgang, Michael J. Role of the malonyl-CoA synthetase ACSF3 in mitochondrial metabolism. Advances in Biological Regulation. 2019-01, 71 [2024-09-03]. PMC 6347522 . PMID 30201289. doi:10.1016/j.jbior.2018.09.002. （原始内容存档于2024-06-12）（英语）.
Bowman, Caitlyn E.; Rodriguez, Susana; Selen Alpergin, Ebru S.; Acoba, Michelle G.; Zhao, Liang; Hartung, Thomas; Claypool, Steven M.; Watkins, Paul A.; Wolfgang, Michael J. The Mammalian Malonyl-CoA Synthetase ACSF3 Is Required for Mitochondrial Protein Malonylation and Metabolic Efficiency. Cell Chemical Biology. 2017-06, 24 (6) [2024-09-03]. PMC 5482780 . PMID 28479296. doi:10.1016/j.chembiol.2017.04.009. （原始内容存档于2023-06-05）（英语）.
Tucci, Sara. Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria. Orphanet Journal of Rare Diseases. 2020-12, 15 (1) [2024-09-03]. ISSN 1750-1172. PMC 6977288 . PMID 31969167. doi:10.1186/s13023-020-1299-7. （原始内容存档于2023-03-21）（英语）.
Mayr, Johannes A.; Feichtinger, René G.; Tort, Frederic; Ribes, Antonia; Sperl, Wolfgang. Lipoic acid biosynthesis defects. Journal of Inherited Metabolic Disease. 2014-07, 37 (4) [2024-09-03]. ISSN 0141-8955. doi:10.1007/s10545-014-9705-8. （原始内容存档于2024-02-17）（英语）.
Monteuuis, Geoffray; Suomi, Fumi; Kerätär, Juha M.; Masud, Ali J.; Kastaniotis, Alexander J. A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3. Biochemical Journal. 2017-11-15, 474 (22) [2024-09-03]. ISSN 0264-6021. doi:10.1042/BCJ20170416. （原始内容存档于2023-06-22）（英语）.
Thompson, G.N.; Walter, J.H.; Bresson, J.-L.; Ford, G.C.; Lyonnet, S.L.; Chalmers, R.A.; Saudubray, J.-M.; Leonard, J.V.; Halliday, D. Sources of propionate in inborn errors of propionate metabolism. Metabolism. 1990-11, 39 (11) [2024-09-01]. doi:10.1016/0026-0495(90)90084-P. （原始内容存档于2022-06-15）（英语）.
Scharinger, Marwa; Kuntz, Marcel; Scharinger, Andreas; Teipel, Jan; Kuballa, Thomas; Walch, Stephan G.; Lachenmeier, Dirk W. Rapid Approach to Determine Propionic and Sorbic Acid Contents in Bread and Bakery Products Using 1H NMR Spectroscopy. Foods. 2021-03-03, 10 (3) [2024-09-04]. ISSN 2304-8158. doi:10.3390/foods10030526. （原始内容存档于2024-07-07）（英语）.
Yamamura, T; Okamoto, Y; Okada, G; Takaishi, Y; Takamura, M; Mantani, A; Kurata, A; Otagaki, Y; Yamashita, H; Yamawaki, S. Association of thalamic hyperactivity with treatment-resistant depression and poor response in early treatment for major depression: a resting-state fMRI study using fractional amplitude of low-frequency fluctuations. Translational Psychiatry. 2016-03-08, 6 (3) [2024-09-04]. ISSN 2158-3188. PMC 4872444 . PMID 26954981. doi:10.1038/tp.2016.18. （原始内容存档于2024-02-03）（英语）.
McLaughlin, B.A; Nelson, D; Silver, I.A; Erecinska, M; Chesselet, M.-F. Methylmalonate toxicity in primary neuronal cultures. Neuroscience. 1998-05, 86 (1) [2024-09-04]. doi:10.1016/S0306-4522(97)00594-0. （原始内容存档于2024-06-06）（英语）.
Kölker, S.; Ahlmeyer, B.; Krieglstein, J.; Hoffmann, G. F. Methylmalonic acid induces excitotoxic neuronal damage in vitro. Journal of Inherited Metabolic Disease. 2000-06, 23 (4) [2024-09-04]. ISSN 0141-8955. doi:10.1023/A:1005631230455. （原始内容存档于2024-07-07）（英语）.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria. Molecular Genetics & Genomic Medicine. 2021-04, 9 (4) [2022-08-06]. ISSN 2324-9269. PMC 8123733 . PMID 33625768. doi:10.1002/mgg3.1621. （原始内容存档于2022-09-21）（英语）.
Thompson, G.N.; Walter, J.H.; Bresson, J.-L.; Ford, G.C.; Lyonnet, S.L.; Chalmers, R.A.; Saudubray, J.-M.; Leonard, J.V.; Halliday, D. Sources of propionate in inborn errors of propionate metabolism. Metabolism. 1990-11, 39 (11) [2024-09-01]. doi:10.1016/0026-0495(90)90084-P. （原始内容存档于2022-06-15）（英语）.
An, Ding; Schneller, Jessica L.; Frassetto, Andrea; Liang, Shi; Zhu, Xuling; Park, Ji-Sun; Theisen, Matt; Hong, Sue-Jean; Zhou, Jenny; Rajendran, Raj; Levy, Becca. Systemic Messenger RNA Therapy as a Treatment for Methylmalonic Acidemia. Cell Reports. 2017-12, 21 (12) [2024-09-01]. PMC 9667413 . PMID 29262333. doi:10.1016/j.celrep.2017.11.081. （原始内容存档于2024-09-05）（英语）.
Martini, Paolo G.V.; Guey, Lin T. A New Era for Rare Genetic Diseases: Messenger RNA Therapy. Human Gene Therapy. 2019-10-01, 30 (10) [2024-09-01]. ISSN 1043-0342. doi:10.1089/hum.2019.090. （原始内容存档于2022-02-24）（英语）.
Brown, G. K.; Scholem, R. D.; Bankier, A.; Danks, D. M. Malonyl coenzyme a decarboxylase deficiency. Journal of Inherited Metabolic Disease. 1984-03, 7 (1) [2024-09-01]. ISSN 0141-8955. doi:10.1007/BF01805615. （原始内容存档于2024-04-20）（英语）.
Ozand, P.T.; Nyhan, W.L.; Al Aqeel, A.; Christodoulou, J. Malonic aciduria. Brain and Development. 1994-11, 16 [2024-09-01]. doi:10.1016/0387-7604(94)90091-4. （原始内容存档于2022-10-22）（英语）.

elsevier.com

linkinghub.elsevier.com

Wehbe, Zeinab; Behringer, Sidney; Alatibi, Khaled; Watkins, David; Rosenblatt, David; Spiekerkoetter, Ute; Tucci, Sara. The emerging role of the mitochondrial fatty-acid synthase (mtFASII) in the regulation of energy metabolism. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 2019-11, 1864 (11) [2022-08-06]. doi:10.1016/j.bbalip.2019.07.012. （原始内容存档于2022-06-19）（英语）.
Sniderman, Lisa C.; Lambert, Marie; Giguère, Robert; Auray-Blais, Christiane; Lemieux, Bernard; Laframboise, Rachel; Rosenblatt, David S.; Treacy, Eileen P. Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program. The Journal of Pediatrics. 1999-06, 134 (6) [2022-07-31]. doi:10.1016/S0022-3476(99)70280-5. （原始内容存档于2018-06-11）（英语）.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart. Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis. Journal of Biological Chemistry. 2011-09, 286 (39) [2022-07-31]. PMC 3190830 . PMID 21846720. doi:10.1074/jbc.M111.291591. （原始内容存档于2022-08-02）（英语）.
Bowman, Caitlyn E.; Wolfgang, Michael J. Role of the malonyl-CoA synthetase ACSF3 in mitochondrial metabolism. Advances in Biological Regulation. 2019-01, 71 [2024-09-03]. PMC 6347522 . PMID 30201289. doi:10.1016/j.jbior.2018.09.002. （原始内容存档于2024-06-12）（英语）.
Bowman, Caitlyn E.; Rodriguez, Susana; Selen Alpergin, Ebru S.; Acoba, Michelle G.; Zhao, Liang; Hartung, Thomas; Claypool, Steven M.; Watkins, Paul A.; Wolfgang, Michael J. The Mammalian Malonyl-CoA Synthetase ACSF3 Is Required for Mitochondrial Protein Malonylation and Metabolic Efficiency. Cell Chemical Biology. 2017-06, 24 (6) [2024-09-03]. PMC 5482780 . PMID 28479296. doi:10.1016/j.chembiol.2017.04.009. （原始内容存档于2023-06-05）（英语）.
Thompson, G.N.; Walter, J.H.; Bresson, J.-L.; Ford, G.C.; Lyonnet, S.L.; Chalmers, R.A.; Saudubray, J.-M.; Leonard, J.V.; Halliday, D. Sources of propionate in inborn errors of propionate metabolism. Metabolism. 1990-11, 39 (11) [2024-09-01]. doi:10.1016/0026-0495(90)90084-P. （原始内容存档于2022-06-15）（英语）.
McLaughlin, B.A; Nelson, D; Silver, I.A; Erecinska, M; Chesselet, M.-F. Methylmalonate toxicity in primary neuronal cultures. Neuroscience. 1998-05, 86 (1) [2024-09-04]. doi:10.1016/S0306-4522(97)00594-0. （原始内容存档于2024-06-06）（英语）.
Thompson, G.N.; Walter, J.H.; Bresson, J.-L.; Ford, G.C.; Lyonnet, S.L.; Chalmers, R.A.; Saudubray, J.-M.; Leonard, J.V.; Halliday, D. Sources of propionate in inborn errors of propionate metabolism. Metabolism. 1990-11, 39 (11) [2024-09-01]. doi:10.1016/0026-0495(90)90084-P. （原始内容存档于2022-06-15）（英语）.
An, Ding; Schneller, Jessica L.; Frassetto, Andrea; Liang, Shi; Zhu, Xuling; Park, Ji-Sun; Theisen, Matt; Hong, Sue-Jean; Zhou, Jenny; Rajendran, Raj; Levy, Becca. Systemic Messenger RNA Therapy as a Treatment for Methylmalonic Acidemia. Cell Reports. 2017-12, 21 (12) [2024-09-01]. PMC 9667413 . PMID 29262333. doi:10.1016/j.celrep.2017.11.081. （原始内容存档于2024-09-05）（英语）.
Ozand, P.T.; Nyhan, W.L.; Al Aqeel, A.; Christodoulou, J. Malonic aciduria. Brain and Development. 1994-11, 16 [2024-09-01]. doi:10.1016/0387-7604(94)90091-4. （原始内容存档于2022-10-22）（英语）.

frontiersin.org

Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan. Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients. Frontiers in Pediatrics. 2021-11-25, 9 [2022-08-06]. ISSN 2296-2360. PMC 8658908 . PMID 34900860. doi:10.3389/fped.2021.751895. （原始内容存档于2022-09-21）.

jkms.org

Lee, Joon Kee; Oh, Arum. Combined Malonic and Methylmalonic Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report. Journal of Korean Medical Science. 2023, 38 (45) [2024-09-01]. ISSN 1011-8934. PMC 10659923 . PMID 37987109. doi:10.3346/jkms.2023.38.e387. （原始内容存档于2024-06-30）（英语）.

liebertpub.com

Martini, Paolo G.V.; Guey, Lin T. A New Era for Rare Genetic Diseases: Messenger RNA Therapy. Human Gene Therapy. 2019-10-01, 30 (10) [2024-09-01]. ISSN 1043-0342. doi:10.1089/hum.2019.090. （原始内容存档于2022-02-24）（英语）.

mayocliniclabs.com

Targeted Genes and Methodology Details for Methylmalonic Aciduria Gene Panel. Mayo Clinic Laboratories. [2024-05-16]. （原始内容存档于2024-05-26）（英语）.

mdpi.com

Scharinger, Marwa; Kuntz, Marcel; Scharinger, Andreas; Teipel, Jan; Kuballa, Thomas; Walch, Stephan G.; Lachenmeier, Dirk W. Rapid Approach to Determine Propionic and Sorbic Acid Contents in Bread and Bakery Products Using 1H NMR Spectroscopy. Foods. 2021-03-03, 10 (3) [2024-09-04]. ISSN 2304-8158. doi:10.3390/foods10030526. （原始内容存档于2024-07-07）（英语）.

modernatx.com

trials.modernatx.com

"A Clinical Trial of a Methylmalonic Acidemia (MMA) Due to MUT Deficiency Treatment for Children and Adults". Moderna. [2024-01-04]. （原始内容存档于2022-02-18）.

nature.com

NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R; O'Brien, Kevin; Hauser, Natalie S. Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. Nature Genetics. 2011-09, 43 (9) [2022-07-31]. ISSN 1061-4036. PMC 3163731 . PMID 21841779. doi:10.1038/ng.908. （原始内容存档于2022-09-21）（英语）.
Yamamura, T; Okamoto, Y; Okada, G; Takaishi, Y; Takamura, M; Mantani, A; Kurata, A; Otagaki, Y; Yamashita, H; Yamawaki, S. Association of thalamic hyperactivity with treatment-resistant depression and poor response in early treatment for major depression: a resting-state fMRI study using fractional amplitude of low-frequency fluctuations. Translational Psychiatry. 2016-03-08, 6 (3) [2024-09-04]. ISSN 2158-3188. PMC 4872444 . PMID 26954981. doi:10.1038/tp.2016.18. （原始内容存档于2024-02-03）（英语）.

nih.gov

ncbi.nlm.nih.gov

de Sain-van der Velden, Monique G. M.; van der Ham, Maria; Jans, Judith J.; Visser, Gepke; Prinsen, Hubertus C. M. T.; Verhoeven-Duif, Nanda M.; van Gassen, Koen L. I.; van Hasselt, Peter M. A New Approach for Fast Metabolic Diagnostics in CMAMMA. Morava, Eva (编). JIMD Reports, Volume 30 30. Berlin, Heidelberg: Springer Berlin Heidelberg. 2016: 15–22 [2022-07-31]. ISBN 978-3-662-53680-3. PMC 5110436 . PMID 26915364. doi:10.1007/8904_2016_531. （原始内容存档于2022-09-22）.
Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A.; Brunel‐Guitton, Catherine; Braverman, Nancy E. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. 2019, 42 (1): 107–116 [2022-08-06]. ISSN 0141-8955. PMID 30740739. S2CID 73436689. doi:10.1002/jimd.12032. （原始内容存档于2022-09-22）（英语）.
NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R; O'Brien, Kevin; Hauser, Natalie S. Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. Nature Genetics. 2011-09, 43 (9) [2022-07-31]. ISSN 1061-4036. PMC 3163731 . PMID 21841779. doi:10.1038/ng.908. （原始内容存档于2022-09-21）（英语）.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan. Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients. Frontiers in Pediatrics. 2021-11-25, 9 [2022-08-06]. ISSN 2296-2360. PMC 8658908 . PMID 34900860. doi:10.3389/fped.2021.751895. （原始内容存档于2022-09-21）.
Gregg, A. R.; Warman, A. W.; Thorburn, D. R.; O'Brien, W. E. Combined malonic and methylmalonic aciduria with normal malonyl-coenzyme A decarboxylase activity: A case supporting multiple aetiologies. Journal of Inherited Metabolic Disease. 1998, 21 (4): 382–390 [2022-08-06]. PMID 9700595. S2CID 20212973. doi:10.1023/A:1005302607897. （原始内容存档于2022-06-15）（英语）.
Witkowski, Andrzej; Thweatt, Jennifer; Smith, Stuart. Mammalian ACSF3 Protein Is a Malonyl-CoA Synthetase That Supplies the Chain Extender Units for Mitochondrial Fatty Acid Synthesis. Journal of Biological Chemistry. 2011-09, 286 (39) [2022-07-31]. PMC 3190830 . PMID 21846720. doi:10.1074/jbc.M111.291591. （原始内容存档于2022-08-02）（英语）.
Lee, Joon Kee; Oh, Arum. Combined Malonic and Methylmalonic Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report. Journal of Korean Medical Science. 2023, 38 (45) [2024-09-01]. ISSN 1011-8934. PMC 10659923 . PMID 37987109. doi:10.3346/jkms.2023.38.e387. （原始内容存档于2024-06-30）（英语）.
Bowman, Caitlyn E.; Wolfgang, Michael J. Role of the malonyl-CoA synthetase ACSF3 in mitochondrial metabolism. Advances in Biological Regulation. 2019-01, 71 [2024-09-03]. PMC 6347522 . PMID 30201289. doi:10.1016/j.jbior.2018.09.002. （原始内容存档于2024-06-12）（英语）.
Bowman, Caitlyn E.; Rodriguez, Susana; Selen Alpergin, Ebru S.; Acoba, Michelle G.; Zhao, Liang; Hartung, Thomas; Claypool, Steven M.; Watkins, Paul A.; Wolfgang, Michael J. The Mammalian Malonyl-CoA Synthetase ACSF3 Is Required for Mitochondrial Protein Malonylation and Metabolic Efficiency. Cell Chemical Biology. 2017-06, 24 (6) [2024-09-03]. PMC 5482780 . PMID 28479296. doi:10.1016/j.chembiol.2017.04.009. （原始内容存档于2023-06-05）（英语）.
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portlandpress.com

Monteuuis, Geoffray; Suomi, Fumi; Kerätär, Juha M.; Masud, Ali J.; Kastaniotis, Alexander J. A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3. Biochemical Journal. 2017-11-15, 474 (22) [2024-09-03]. ISSN 0264-6021. doi:10.1042/BCJ20170416. （原始内容存档于2023-06-22）（英语）.

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wiley.com

onlinelibrary.wiley.com

Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A.; Brunel‐Guitton, Catherine; Braverman, Nancy E. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. 2019, 42 (1): 107–116 [2022-08-06]. ISSN 0141-8955. PMID 30740739. S2CID 73436689. doi:10.1002/jimd.12032. （原始内容存档于2022-09-22）（英语）.
Mayr, Johannes A.; Feichtinger, René G.; Tort, Frederic; Ribes, Antonia; Sperl, Wolfgang. Lipoic acid biosynthesis defects. Journal of Inherited Metabolic Disease. 2014-07, 37 (4) [2024-09-03]. ISSN 0141-8955. doi:10.1007/s10545-014-9705-8. （原始内容存档于2024-02-17）（英语）.
Kölker, S.; Ahlmeyer, B.; Krieglstein, J.; Hoffmann, G. F. Methylmalonic acid induces excitotoxic neuronal damage in vitro. Journal of Inherited Metabolic Disease. 2000-06, 23 (4) [2024-09-04]. ISSN 0141-8955. doi:10.1023/A:1005631230455. （原始内容存档于2024-07-07）（英语）.
Gabriel, Marie Cosette; Rice, Stephanie M.; Sloan, Jennifer L.; Mossayebi, Matthew H.; Venditti, Charles P.; Al‐Kouatly, Huda B. Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria. Molecular Genetics & Genomic Medicine. 2021-04, 9 (4) [2022-08-06]. ISSN 2324-9269. PMC 8123733 . PMID 33625768. doi:10.1002/mgg3.1621. （原始内容存档于2022-09-21）（英语）.
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doi.wiley.com

Gregg, A. R.; Warman, A. W.; Thorburn, D. R.; O'Brien, W. E. Combined malonic and methylmalonic aciduria with normal malonyl-coenzyme A decarboxylase activity: A case supporting multiple aetiologies. Journal of Inherited Metabolic Disease. 1998, 21 (4): 382–390 [2022-08-06]. PMID 9700595. S2CID 20212973. doi:10.1023/A:1005302607897. （原始内容存档于2022-06-15）（英语）.

worldcat.org

Levtova, Alina; Waters, Paula J.; Buhas, Daniela; Lévesque, Sébastien; Auray‐Blais, Christiane; Clarke, Joe T.R.; Laframboise, Rachel; Maranda, Bruno; Mitchell, Grant A.; Brunel‐Guitton, Catherine; Braverman, Nancy E. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. 2019, 42 (1): 107–116 [2022-08-06]. ISSN 0141-8955. PMID 30740739. S2CID 73436689. doi:10.1002/jimd.12032. （原始内容存档于2022-09-22）（英语）.
NIH Intramural Sequencing Center Group; Sloan, Jennifer L; Johnston, Jennifer J; Manoli, Irini; Chandler, Randy J; Krause, Caitlin; Carrillo-Carrasco, Nuria; Chandrasekaran, Suma D; Sysol, Justin R; O'Brien, Kevin; Hauser, Natalie S. Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. Nature Genetics. 2011-09, 43 (9) [2022-07-31]. ISSN 1061-4036. PMC 3163731 . PMID 21841779. doi:10.1038/ng.908. （原始内容存档于2022-09-21）（英语）.
Wang, Ping; Shu, Jianbo; Gu, Chunyu; Yu, Xiaoli; Zheng, Jie; Zhang, Chunhua; Cai, Chunquan. Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients. Frontiers in Pediatrics. 2021-11-25, 9 [2022-08-06]. ISSN 2296-2360. PMC 8658908 . PMID 34900860. doi:10.3389/fped.2021.751895. （原始内容存档于2022-09-21）.
Alfares, A.; Nunez, L. D.; Al-Thihli, K.; Mitchell, J.; Melancon, S.; Anastasio, N.; Ha, K. C. H.; Majewski, J.; Rosenblatt, D. S.; Braverman, N. Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype. Journal of Medical Genetics. 2011-09-01, 48 (9) [2022-08-06]. ISSN 0022-2593. doi:10.1136/jmedgenet-2011-100230. （原始内容存档于2022-06-15）（英语）.
Lee, Joon Kee; Oh, Arum. Combined Malonic and Methylmalonic Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report. Journal of Korean Medical Science. 2023, 38 (45) [2024-09-01]. ISSN 1011-8934. PMC 10659923 . PMID 37987109. doi:10.3346/jkms.2023.38.e387. （原始内容存档于2024-06-30）（英语）.
Tucci, Sara. Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria. Orphanet Journal of Rare Diseases. 2020-12, 15 (1) [2024-09-03]. ISSN 1750-1172. PMC 6977288 . PMID 31969167. doi:10.1186/s13023-020-1299-7. （原始内容存档于2023-03-21）（英语）.
Mayr, Johannes A.; Feichtinger, René G.; Tort, Frederic; Ribes, Antonia; Sperl, Wolfgang. Lipoic acid biosynthesis defects. Journal of Inherited Metabolic Disease. 2014-07, 37 (4) [2024-09-03]. ISSN 0141-8955. doi:10.1007/s10545-014-9705-8. （原始内容存档于2024-02-17）（英语）.
Monteuuis, Geoffray; Suomi, Fumi; Kerätär, Juha M.; Masud, Ali J.; Kastaniotis, Alexander J. A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3. Biochemical Journal. 2017-11-15, 474 (22) [2024-09-03]. ISSN 0264-6021. doi:10.1042/BCJ20170416. （原始内容存档于2023-06-22）（英语）.
Scharinger, Marwa; Kuntz, Marcel; Scharinger, Andreas; Teipel, Jan; Kuballa, Thomas; Walch, Stephan G.; Lachenmeier, Dirk W. Rapid Approach to Determine Propionic and Sorbic Acid Contents in Bread and Bakery Products Using 1H NMR Spectroscopy. Foods. 2021-03-03, 10 (3) [2024-09-04]. ISSN 2304-8158. doi:10.3390/foods10030526. （原始内容存档于2024-07-07）（英语）.
Yamamura, T; Okamoto, Y; Okada, G; Takaishi, Y; Takamura, M; Mantani, A; Kurata, A; Otagaki, Y; Yamashita, H; Yamawaki, S. Association of thalamic hyperactivity with treatment-resistant depression and poor response in early treatment for major depression: a resting-state fMRI study using fractional amplitude of low-frequency fluctuations. Translational Psychiatry. 2016-03-08, 6 (3) [2024-09-04]. ISSN 2158-3188. PMC 4872444 . PMID 26954981. doi:10.1038/tp.2016.18. （原始内容存档于2024-02-03）（英语）.
Kölker, S.; Ahlmeyer, B.; Krieglstein, J.; Hoffmann, G. F. Methylmalonic acid induces excitotoxic neuronal damage in vitro. Journal of Inherited Metabolic Disease. 2000-06, 23 (4) [2024-09-04]. ISSN 0141-8955. doi:10.1023/A:1005631230455. （原始内容存档于2024-07-07）（英语）.
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