Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease

This study was undertaken to examine the association between the level of heteroplasmy for the mutation C3256T in human white blood cells and the extent of carotid atherosclerosis, as well as the presence of coronary heart disease (CHD), the major clinical manifestation of atherosclerosis. Totally,...

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Detalles Bibliográficos
Autores principales: Sobenin, Igor A., Sazonova, Margarita A., Ivanova, Maria M., Zhelankin, Andrey V., Myasoedova, Veronika A., Postnov, Anton Y., Nurbaev, Serik D., Bobryshev, Yuri V., Orekhov, Alexander N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462756/
https://www.ncbi.nlm.nih.gov/pubmed/23056349
http://dx.doi.org/10.1371/journal.pone.0046573

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462756/
https://www.ncbi.nlm.nih.gov/pubmed/23056349
http://dx.doi.org/10.1371/journal.pone.0046573

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