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Mutations of mitochondrial genome in carotid atherosclerosis
With aim of detection the spectrum of mitochondrial DNA mutations in patients with carotid atherosclerosis from Moscow Region, we used a Roche 454 high-throughput sequencing of the whole mitochondrial genome. We have found that the presence of a number of homoplasmic mitochondrial DNA mutations in g...
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| Gepubliceerd in: | Front Genet |
|---|---|
| Hoofdauteurs: | , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Frontiers Media S.A.
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4365735/ https://ncbi.nlm.nih.gov/pubmed/25852749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2015.00111 |
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