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This disorder is caused by an inherited deficiency of glutaryl-CoA dehydrogenase, which is involved in the catabolic pathways of L-lysine, L-hydroxylysine and L-tryptophan (97)
doi:10.1016/j.coemr.2021.03.021

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ISBN-10 0323825400, ISBN-13 978-0323825405 Technical Reports Mitchell, K., Rosenberg, J., Brizan-St
Additionally, if treated before symptoms develop, even infants predicted to have SMA type II (genetically diagnosed but asymptomatic) would be able to walk independently [137,145]

Puerarin alleviates atherosclerosis via the inhibition of Prevotella copri and its trimethylamine production