Therapeutic concepts in succinate semialdehyde dehydrogenase (SSADH; ALDH5a1) deficiency (γ-hydroxybutyric aciduria). Hypotheses evolved from 25 years of patient evaluation, studies in Aldh5a1 −/− mice and characterization of γ-hydroxybutyric acid pharmacology

Author: Knerr I.   Pearl P.   Bottiglieri T.   Carter Snead O.   Jakobs C.   Gibson K.  

Publisher: Springer Publishing Company

ISSN: 0141-8955

Source: Journal of Inherited Metabolic Disease, Vol.30, Iss.3, 2007-06, pp. : 279-294

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