Background: Methylmalonic acidemia (MMA) is a rare autosomal recessive metabolic disorder resulting from a genetic defect in methylmalonyl-CoA mutase (MCM) or a defect in the biosynthesis of its cofactor. adenosyl-cobalamin (AdoCbl). The disease is caused by a mutation in six main genes (MUT. MMAA. https://foldlyers.shop/product-category/displayport-to-dvi-i/
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