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Genetic and Genomic Systems to Study Methylmalonic Acidemia

Methylmalonic acidemia (MMAemia) is the biochemical hallmark of a group of genetic metabolic disorders that share a common defect in the ability to convert methylmalonyl-CoA into succinyl-CoA. This disorder is due to either a mutant methylmalonyl-CoA mutase apoenzyme or impaired synthesis of adenosy...

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Detalhes bibliográficos
Main Authors: Chandler, R.J., Venditti, C. P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2657357/
https://ncbi.nlm.nih.gov/pubmed/16182581
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2005.07.020
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