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Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲二酸血症是由于甲二酰A变位或其苷钴胺素缺陷所致一种遗传性代谢疾病。

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Prosthetic enzyme of mutase, catalyze reactions of group, mainly methyl, metachoresis in the interior of substrate molecule.

变位，催化底物分子内团(主要为甲)变位反应。

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3G, 401(K), a,

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