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Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases
Mitochondrial DNA (mtDNA) is highly polymorphic at the population level, and specific mtDNA variants affect mitochondrial function. With emerging evidence that mitochondrial mechanisms are central to common human diseases, it is plausible that mtDNA variants contribute to the “missing heritability”...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4031051/ https://ncbi.nlm.nih.gov/pubmed/24852434 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1004369 |
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