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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]
10.1016/j.neuroscience.2014.11.025 [DOI] [PubMed] [Google Scholar] 94.Peng S, Li W, Lv L, Zhang Z, Zhan X
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10.1016/j.molcel.2018.01.010 113 XiongX.WenY
Ynsadiet L-Carnitine 1500Mg
[DOI] [PubMed] [Google Scholar] 115.Chilelli N., Ragazzi E., Valentini R., Cosma C., Ferraresso S., Lapolla A., Sartore G
