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Respiratory chain complex I deficiency caused by mitochondrial DNA mutations
Defects of the mitochondrial respiratory chain are associated with a diverse spectrum of clinical phenotypes, and may be caused by mutations in either the nuclear or the mitochondrial genome (mitochondrial DNA (mtDNA)). Isolated complex I deficiency is the most common enzyme defect in mitochondrial...
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| Autors principals: | , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3137493/ https://ncbi.nlm.nih.gov/pubmed/21364701 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.18 |
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