Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease

Many lines of evidence implicate mitochondria in phenotypic variation: (a) rare mutations in mitochondrial proteins cause metabolic, neurological, and muscular disorders; (b) alterations in oxidative phosphorylation are characteristic of type 2 diabetes, Parkinson disease, Huntington disease, and ot...

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Autores principales: Saxena, Richa, de Bakker, Paul I. W., Singer, Karyn, Mootha, Vamsi, Burtt, Noël, Hirschhorn, Joel N., Gaudet, Daniel, Isomaa, Bo, Daly, Mark J., Groop, Leif, Ardlie, Kristin G., Altshuler, David
Formato: Artigo
Lenguaje:Inglês
Publicado: The American Society of Human Genetics 2006
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1474138/
https://ncbi.nlm.nih.gov/pubmed/16773565
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