Inherited disorders of GABA metabolism
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00711902
Reference39 articles.
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2. Bartsch K, von Johnn-Marteville A, Schulz A (1990) Molecular analysis of two genes of theEscherichia coli gab cluster: nucleotide sequence of the glutamate: succinic semialdehyde transaminase gene (gabT) and characterization of the succinic semialdehyde dehydrogenase gene (gabD).J Bacteriol 172: 7035?7042.
3. Brown GK, Cromby CH, Manning NJ, Pollitt RJ (1987) Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of ?-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial ?-oxidation.J Inher Metab Dis 10: 367?375.
4. Bu D-F, Erlander MG, Hitz BC et al (1992) Two human glutamate decarboxylases, 65-kDa GAD and 67-kDa GAD, are each encoded by a single gene.Proc Natl Acad Sci USA 89: 2115?2119.
5. Carchon HA, Jaeken J, Jansen E, Eggermont E (1991) Reference values for free gammaminobutyric acid determined by ion-exchange chromatography and fluorescence detection in the cerebrospinal fluid of children.Clin Chim Acta 201: 83?88.
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