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Description
Glutaryl-CoA dehydrogenase (GCDH) deficiency is an inborn error of lysine and tryptophan metabolism that results in increased formation and excretion of glutaric acid (GA), 3-hydroxyglutaric acid (3-OH-GA), glutaconic acid and glutarylcarnitine [82]

[DOI] [PubMed] [Google Scholar] 116.Kunnecke B, Cerdan S, Seelig J

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Essays Biochem

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