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...

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Bibliographic Details
Main Authors: S Ун Nikulina, V A Shulman, Yu V Vorotnikova, V P Puzyrev, Т V Kosyankova, M V Golubenko
Format: Article
Language:Russian
Published: "Consilium Medicum" Publishing house 2003-10-01
Series:Терапевтический архив
Subjects:
Online Access:https://ter-arkhiv.ru/0040-3660/article/view/29676