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Falk MH, Meier T, Issels RD, Brielmeier M, Scheffer B, Bornkamm GW
For AOD-9604, use 1mL of water per 2mg to create a 2mg/mL solution
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: 10.1007/s44163-025-00420-8 170
no adverse outcomes have been attributed to nursing infants, yet unnecessary exposure should be avoided
Modern lifestyle habits, unhealthy eating routines, stress, and lack of physical activity can affect metabolism and body fitness
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