MMAB ELISA试剂盒
(Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011].
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Aliases for MMAB ELISA试剂盒
methylmalonic aciduria (cobalamin deficiency) cblB type (MMAB) ELISA试剂盒methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) (Mmab) ELISA试剂盒
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