Identification of a Familial Mutation Associated with GABA-Transaminase Deficiency Disease by Lali K. Medina-Kauwe, W.L. Nyhan, K.M. Gibson, A.J. Tobin

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Post-translational regulation of mevalonate kinase by intermediates of the cholesterol and nonsterol isoprene biosynthetic pathways by D D Hinson, K L Chambliss, M J Toth, R D Tanaka, K M Gibson

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Seizure evolution and amino acid imbalances in murine succinate semialdehyde dehydrogenase (SSADH) deficiency by M Gupta, M Polinsky, H Senephansiri, O.C Snead, E.E.W Jansen, C Jakobs, K.M Gibson

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Preclinical tissue distribution and metabolic correlations of vigabatrin, an antiepileptic drug associated with potential use‐limiting visual field defects by Dana C. Walters, Erwin E. W. Jansen, Garrett R. Ainslie, Gajja S. Salomons, Madalyn N. Brown, Michelle A. Schmidt, Jean‐Baptiste Roullet, K. M. Gibson

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Targeted screening of succinic semialdehyde dehydrogenase deficiency (SSADHD) employing an enzymatic assay for γ-hydroxybutyric acid (GHB) in biofluids by C. Wernli, S. Finochiaro, C. Volken, H. Andresen-Streichert, A. Buettler, D. Gygax, G.S. Salomons, E.E. Jansen, G.R. Ainslie, K.R. Vogel, K.M. Gibson

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