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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Detalles Bibliográficos
Publicado en:Front Genet
Main Authors: Sazonova, Margarita A., Zhelankin, Andrey V., Barinova, Valeria A., Sinyov, Vasily V., Khasanova, Zukhra B., Postnov, Anton Y., Orekhov, Alexander N., Bobryshev, Yuri V., Sobenin, Igor A.
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2015
Assuntos:
Pediatrics
Acceso en liña: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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