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3-Methylcrotonylglycinuria 3-Methylcrotonylglycinuria is a disorder of leucine catabolism that results from defects in either of the two subunits of the biotin-requiring enzyme, 3-methylcrotonyl-CoA carboxylase (3MCC)

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10.1016/s0022-3956(96)00050-7 J

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En cualquier caso, es una sustancia natural producida por nuestro propio organismo, por eso no tiene un gran nmero de efectos secundarios

Further studies, including prospective study designs and more diverse populations, are required to determine causal associations between G6PD deficiency and ADHD risk and elucidate underlying biological mechanisms