Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲丙二酸血症是由于甲丙二酰A变位或其苷钴胺素缺陷所致的一种遗传性代谢疾病。
Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.
变位的,化底物分子内团(主要为甲)的变位反应。
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