MMACHC (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "MMACHC" in English language version.

Last modified: 05:46:40, 15 June 2026 (UTC)

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doi.org (Global: 2^nd place; English: 2^nd place)

Lerner-Ellis JP, Tirone JC, Pawelek PD, Doré C, Atkinson JL, Watkins D, et al. (January 2006). "Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type". Nature Genetics. 38 (1): 93–100. doi:10.1038/ng1683. PMID 16311595. S2CID 7688576.
Ben-Omran TI, Wong H, Blaser S, Feigenbaum A (May 2007). "Late-onset cobalamin-C disorder: a challenging diagnosis". American Journal of Medical Genetics. Part A. 143A (9): 979–984. doi:10.1002/ajmg.a.31671. PMID 17431913. S2CID 19791175.
Morel CF, Lerner-Ellis JP, Rosenblatt DS (August 2006). "Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations". Molecular Genetics and Metabolism. 88 (4): 315–321. doi:10.1016/j.ymgme.2006.04.001. PMID 16714133.
Tsai AC, Morel CF, Scharer G, Yang M, Lerner-Ellis JP, Rosenblatt DS, et al. (October 2007). "Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance". American Journal of Medical Genetics. Part A. 143A (20): 2430–2434. doi:10.1002/ajmg.a.31932. PMID 17853453. S2CID 19372503.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Luciana Hannibal, Jihoe Kim, Nicola E. Brasch, Sihe Wang, David S. Rosenblatt, Ruma Banerjee, and Donald W. Jacobsen (August 2009). "Processing of alkylcobalamins in mammalian cells: a role for the MMACHC (cblC) gene product". Mol Genet Metab. 2009 Aug; 97(4): 260–266.
Quadros, EV. "Advances in the Understanding of Cobalamin Assimilation and Metabolism". Br J Haematol. 2010 Jan; 148(2): 195–204.
Sloan JL, Carrillo N, Adams D, Venditti CP (1993). "Disorders of Intracellular Cobalamin Metabolism". In Adam MP, Feldman J, Mirzaa GM, Pagon RA (eds.). GeneReviews^®. Seattle (WA): University of Washington, Seattle. PMID 20301503. Retrieved 2024-02-24.

Lerner-Ellis JP, Tirone JC, Pawelek PD, Doré C, Atkinson JL, Watkins D, et al. (January 2006). "Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type". Nature Genetics. 38 (1): 93–100. doi:10.1038/ng1683. PMID 16311595. S2CID 7688576.
Ben-Omran TI, Wong H, Blaser S, Feigenbaum A (May 2007). "Late-onset cobalamin-C disorder: a challenging diagnosis". American Journal of Medical Genetics. Part A. 143A (9): 979–984. doi:10.1002/ajmg.a.31671. PMID 17431913. S2CID 19791175.
Morel CF, Lerner-Ellis JP, Rosenblatt DS (August 2006). "Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations". Molecular Genetics and Metabolism. 88 (4): 315–321. doi:10.1016/j.ymgme.2006.04.001. PMID 16714133.
Tsai AC, Morel CF, Scharer G, Yang M, Lerner-Ellis JP, Rosenblatt DS, et al. (October 2007). "Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance". American Journal of Medical Genetics. Part A. 143A (20): 2430–2434. doi:10.1002/ajmg.a.31932. PMID 17853453. S2CID 19372503.
Sloan JL, Carrillo N, Adams D, Venditti CP (1993). "Disorders of Intracellular Cobalamin Metabolism". In Adam MP, Feldman J, Mirzaa GM, Pagon RA (eds.). GeneReviews^®. Seattle (WA): University of Washington, Seattle. PMID 20301503. Retrieved 2024-02-24.

Lerner-Ellis JP, Tirone JC, Pawelek PD, Doré C, Atkinson JL, Watkins D, et al. (January 2006). "Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type". Nature Genetics. 38 (1): 93–100. doi:10.1038/ng1683. PMID 16311595. S2CID 7688576.
Ben-Omran TI, Wong H, Blaser S, Feigenbaum A (May 2007). "Late-onset cobalamin-C disorder: a challenging diagnosis". American Journal of Medical Genetics. Part A. 143A (9): 979–984. doi:10.1002/ajmg.a.31671. PMID 17431913. S2CID 19791175.
Tsai AC, Morel CF, Scharer G, Yang M, Lerner-Ellis JP, Rosenblatt DS, et al. (October 2007). "Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance". American Journal of Medical Genetics. Part A. 143A (20): 2430–2434. doi:10.1002/ajmg.a.31932. PMID 17853453. S2CID 19372503.