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甲基丙二酸尿症cblA抗体
半岛bd体育手机客户端 介绍
靶标:
Mmaa 半岛bd体育手机客户端 别名: 2810018E08Rik; AI840684; Mmaa; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria type A homolog, mitochondrial; 甲基丙二酸尿症cblA; 背景信息:
The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008].
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