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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]

Numbness, pins, and needles Tingling in the hands, lips, and other extremities may indicate insufficient vitamin B-12

The copper tripeptide L-alanyl-L-histidyl-L-lysine (Ala-His-Lys) complexed with copper, also called Copper Tripeptide-3, in the same copper-tripeptide family as GHK-Cu