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29. Murine succinate semialdehyde dehydrogenase (SSADH) deficiency, a heritable disorder of GABA metabolism with epileptic phenotype. Gibson KM; Jakobs C; Pearl PL; Snead OC IUBMB Life; 2005 Sep; 57(9):639-44. PubMed ID: 16203683 [TBL] [Abstract][Full Text] [Related]
30. Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolism. Malaspina P; Roullet JB; Pearl PL; Ainslie GR; Vogel KR; Gibson KM Neurochem Int; 2016 Oct; 99():72-84. PubMed ID: 27311541 [TBL] [Abstract][Full Text] [Related]
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34. Biomarkers, metabonomics, and drug development: can inborn errors of metabolism help in understanding drug toxicity? Vangala S; Tonelli A AAPS J; 2007 Jul; 9(3):E284-97. PubMed ID: 17915830 [TBL] [Abstract][Full Text] [Related]
35. Succinic semialdehyde dehydrogenase deficiency in siblings: clinical heterogeneity and response to early treatment. Peters H; Cleary M; Boneh A J Inherit Metab Dis; 1999 Apr; 22(2):198-9. PubMed ID: 10234622 [No Abstract] [Full Text] [Related]
36. 4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism. Gibson KM; Hoffmann GF; Hodson AK; Bottiglieri T; Jakobs C Neuropediatrics; 1998 Feb; 29(1):14-22. PubMed ID: 9553943 [TBL] [Abstract][Full Text] [Related]