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Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6.

Methylmalonyl CoA mutase (MCM) catalyzes an essential step in the degradation of several branch-chain amino acids and odd-chain fatty acids. Deficiency of this apoenzyme causes the mut form of methylmalonic acidemia, an often fatal disorder of organic acid metabolism. An MCM cDNA has recently been o...

詳細記述

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書誌詳細
主要な著者: Ledley, F D, Lumetta, M R, Zoghbi, H Y, VanTuinen, P, Ledbetter, S A, Ledbetter, D H
フォーマット: Artigo
言語:Inglês
出版事項: 1988
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715214/
https://ncbi.nlm.nih.gov/pubmed/2897160
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