Mitochondrial Genome Mutations Associated with Myocardial Infarction

Myocardial infarction is one of the clinical manifestations of coronary heart disease. In some cases, the cause of myocardial infarction may be atherosclerotic plaques which occurred in the human aorta. The association of mtDNA mutations with atherosclerotic lesions in human arteries was previously...

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Detalles Bibliográficos
Autores principales: Sazonova, Margarita A., Ryzhkova, Anastasia I., Sinyov, Vasily V., Galitsyna, Elena V., Melnichenko, Alexandra A., Demakova, Natalya A., Sobenin, Igor A., Shkurat, Tatiana P., Orekhov, Alexander N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835263/
https://www.ncbi.nlm.nih.gov/pubmed/29670672
http://dx.doi.org/10.1155/2018/9749457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835263/
https://www.ncbi.nlm.nih.gov/pubmed/29670672
http://dx.doi.org/10.1155/2018/9749457

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