ASSOCIATION OF MUTATIONS IN THE MITOCHONDRIAL GENOME WITH CORONARY AND CAROTID ATHEROSCLEROTIC LESIONS

ASSOCIATION OF MUTATIONS IN THE MITOCHONDRIAL GENOME WITH CORONARY AND CAROTID ATHEROSCLEROTIC LESIONS

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Objective: to study the association of C3256T, G13 513A, G14 846A, and G12 315A mutations in the mitochondrial genome with the presence and degree of coronary and carotid atherosclerotic lesions.Subjects and methods. The investigation enrolled 193 patients (mean age 54.6 ± 9.5 years), including 154...

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Bibliographic Details
Main Authors: L. A. Smirnova, Z. B. Khasanova, M. V. Ezhov, T. Yu. Polevaya, Yu. G. Matchin, T. V. Balakhonova, I. A. Sobenin, A. Yu. Postnov
Format: Article
Language:Russian
Published: ABV-press 2014-11-01
Series:Klinicist
Subjects:
atherosclerosis
mutations
mitochondrial genome
mitochondrial deoxyribonucleic acid
heteroplasmy
risk factors
Online Access:https://klinitsist.abvpress.ru/Klin/article/view/145

Internet

https://klinitsist.abvpress.ru/Klin/article/view/145

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