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Deep Sequencing of the Mitochondrial Genome Reveals Common Heteroplasmic Sites in NADH Dehydrogenase Genes
Increasing evidence implicates mitochondrial dysfunction in aging and age-related conditions. But little is known about the molecular basis for this connection. A possible cause may be mutations in the mitochondrial DNA (mtDNA), which are often heteroplasmic – the joint presence of different alleles...
Gorde:
| Argitaratua izan da: | Hum Genet |
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| Egile Nagusiak: | , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6335583/ https://ncbi.nlm.nih.gov/pubmed/29423652 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-018-1873-4 |
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