https://hydroxyureainhibitor.c....om/a-multi-purpose-o
Multiple-CoA dehydrogenase deficiency (MADD) is an inborn disorder of fatty acid and amino acid metabolic process due to mutations within the genes encoding for real human electron transfer flavoprotein (ETF) and its particular partner electron transfer flavoproteinubiquinone oxidoreductase (ETFQO). Albeit a rare condition, extensive newborn testing programs added to a wider protection of MADD genotypes. However, the impact of non-lethal mutations on ETFQO purpose continues to be barely reco
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