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...

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Detalhes bibliográficos
Main Authors: Ledley, F D, Lumetta, M R, Zoghbi, H Y, VanTuinen, P, Ledbetter, S A, Ledbetter, D H
Formato: Artigo
Idioma:Inglês
Publicado em: 1988
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715214/
https://ncbi.nlm.nih.gov/pubmed/2897160
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