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Description
Acta 1831 , 291299 (2013)

[DOI] [PubMed] [Google Scholar] 383.Cao, Z

MADD is a disorder that results from mutations in either of the two genes that encode the protein components of the heterodimeric complex identified as electron transfer flavoprotein (ETF) or the gene encoding electron transfer flavoprotein dehydrogenase (encoded by the ETFDH gene)

Vitamina C, vitamina E, zinco, selnio, coenzima Q10, L-carnitina, cido flico e N-acetilcistena, sempre sob orientao mdica
