عوز نازع هيدروجين ألدهيد السكسينيك النصفي (Arabic Wikipedia)

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Chambliss, K. L.؛ Hinson, D. D.؛ Trettel, F.؛ Malaspina, P.؛ Novelletto, A.؛ Jakobs, C.؛ Gibson, K. M. (1998). "Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)". American Journal of Human Genetics. ج. 63 ع. 2: 399–408. DOI:10.1086/301964. PMC:1377305. PMID:9683595.
Pearl, P. L.؛ Novotny, E. J.؛ Acosta, M. T.؛ Jakobs, C.؛ Gibson, K. M. (2003). "Succinic semialdehyde dehydrogenase deficiency in children and adults". Annals of Neurology. 54 Suppl 6: S73–80. DOI:10.1002/ana.10629. PMID:12891657. S2CID:34085564.
Jakobs, C.؛ Jaeken، J.؛ Gibson، K. M. (1993). "Inherited disorders of GABA metabolism". Journal of Inherited Metabolic Disease. ج. 16 ع. 4: 704–715. DOI:10.1007/BF00711902. PMC:3675887. PMID:8412016.
Pearl, P. L.؛ Gibson, K. M. (أبريل 2004). "Clinical aspects of the disorders of GABA metabolism in children". Current Opinion in Neurology. ج. 17 ع. 2: 107–113. DOI:10.1097/00019052-200404000-00005. ISSN:1350-7540. PMID:15021235. S2CID:24090637.
Gibson, K. M.؛ Schor، D. S.؛ Gupta، M.؛ Guerand، W. S.؛ Senephansiri، H.؛ Burlingame، T. G.؛ Bartels، H.؛ Hogema، B. M.؛ وآخرون (2002). "Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenase". Journal of Neurochemistry. ج. 81 ع. 1: 71–79. DOI:10.1046/j.1471-4159.2002.00784.x. PMID:12067239. S2CID:27277845.

Chambliss, K. L.؛ Hinson, D. D.؛ Trettel, F.؛ Malaspina, P.؛ Novelletto, A.؛ Jakobs, C.؛ Gibson, K. M. (1998). "Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)". American Journal of Human Genetics. ج. 63 ع. 2: 399–408. DOI:10.1086/301964. PMC:1377305. PMID:9683595.
Pearl, P. L.؛ Novotny, E. J.؛ Acosta, M. T.؛ Jakobs, C.؛ Gibson, K. M. (2003). "Succinic semialdehyde dehydrogenase deficiency in children and adults". Annals of Neurology. 54 Suppl 6: S73–80. DOI:10.1002/ana.10629. PMID:12891657. S2CID:34085564.
Jakobs, C.؛ Jaeken، J.؛ Gibson، K. M. (1993). "Inherited disorders of GABA metabolism". Journal of Inherited Metabolic Disease. ج. 16 ع. 4: 704–715. DOI:10.1007/BF00711902. PMC:3675887. PMID:8412016.
Pearl, P. L.؛ Gibson, K. M. (أبريل 2004). "Clinical aspects of the disorders of GABA metabolism in children". Current Opinion in Neurology. ج. 17 ع. 2: 107–113. DOI:10.1097/00019052-200404000-00005. ISSN:1350-7540. PMID:15021235. S2CID:24090637.
Gibson, K. M.؛ Schor، D. S.؛ Gupta، M.؛ Guerand، W. S.؛ Senephansiri، H.؛ Burlingame، T. G.؛ Bartels، H.؛ Hogema، B. M.؛ وآخرون (2002). "Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenase". Journal of Neurochemistry. ج. 81 ع. 1: 71–79. DOI:10.1046/j.1471-4159.2002.00784.x. PMID:12067239. S2CID:27277845.

Chambliss, K. L.؛ Hinson, D. D.؛ Trettel, F.؛ Malaspina, P.؛ Novelletto, A.؛ Jakobs, C.؛ Gibson, K. M. (1998). "Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)". American Journal of Human Genetics. ج. 63 ع. 2: 399–408. DOI:10.1086/301964. PMC:1377305. PMID:9683595.
Jakobs, C.؛ Jaeken، J.؛ Gibson، K. M. (1993). "Inherited disorders of GABA metabolism". Journal of Inherited Metabolic Disease. ج. 16 ع. 4: 704–715. DOI:10.1007/BF00711902. PMC:3675887. PMID:8412016.

Pearl, P. L.؛ Novotny, E. J.؛ Acosta, M. T.؛ Jakobs, C.؛ Gibson, K. M. (2003). "Succinic semialdehyde dehydrogenase deficiency in children and adults". Annals of Neurology. 54 Suppl 6: S73–80. DOI:10.1002/ana.10629. PMID:12891657. S2CID:34085564.
Pearl, P. L.؛ Gibson, K. M. (أبريل 2004). "Clinical aspects of the disorders of GABA metabolism in children". Current Opinion in Neurology. ج. 17 ع. 2: 107–113. DOI:10.1097/00019052-200404000-00005. ISSN:1350-7540. PMID:15021235. S2CID:24090637.
Gibson, K. M.؛ Schor، D. S.؛ Gupta، M.؛ Guerand، W. S.؛ Senephansiri، H.؛ Burlingame، T. G.؛ Bartels، H.؛ Hogema، B. M.؛ وآخرون (2002). "Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenase". Journal of Neurochemistry. ج. 81 ع. 1: 71–79. DOI:10.1046/j.1471-4159.2002.00784.x. PMID:12067239. S2CID:27277845.

Pearl, P. L.؛ Gibson, K. M. (أبريل 2004). "Clinical aspects of the disorders of GABA metabolism in children". Current Opinion in Neurology. ج. 17 ع. 2: 107–113. DOI:10.1097/00019052-200404000-00005. ISSN:1350-7540. PMID:15021235. S2CID:24090637.