Polymorphismof non-coding sites of human mitochondrial genome andprimary disorders of cardiac conduction
Aim. Analysis of associations between idiopathic disturbances of cardiac conduction (DCC) and polymorphism of mitochondrial genome. Material and methods. A family examination was performed in 431 probands with various DCC and 1347 relatives of the first, second and third degree of kinship (the study...
Main Authors: | S Ун Nikulina, V A Shulman, Yu V Vorotnikova, V P Puzyrev, Т V Kosyankova, M V Golubenko |
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Format: | Article |
Language: | Russian |
Published: |
"Consilium Medicum" Publishing house
2003-10-01
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Series: | Терапевтический архив |
Subjects: | |
Online Access: | https://ter-arkhiv.ru/0040-3660/article/view/29676 |
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