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doi: 10.1016/j.kint.2024.06.022 19 VerkerkeARPShiXLiMHiguchiYYamamuroTKatohDet al

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]

The mechanistic underpinnings of choline-mediated regulation of lymphocytes, including B, T, and NK cells, remain insufficiently defined

H., She, Q., and Yin, Y

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