Methylmalonic aciduria cblB type
Overview
Methylmalonic aciduria (cobalamin deficiency) cblB type, also known as MMAB, is a human gene
Causes
Methylmalonic acidemia is an inherited disorder in which the body is unable to process certain proteins and fats (lipids) properly. Methylmalonic acidemia is a disorder of amino acid metabolism, involving a defect in the conversion of methylmalonyl-coenzyme A (CoA) to succinyl-CoA by methylmalonyl-CoA mutase.