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human ALDH5A1 protein

deficiency in SSADH causes 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter 4-aminobutyric acid (GABA); RefSeq NM_001080
Also Known As:
ALDH5A1 protein, human; SSADH protein, human; aldehyde dehydrogenase 5 family, member A1 (succinate-semialdehyde dehydrogenase), human
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Bio-Agent Context: Research Results