MOLECULAR GENETIC AND CLINICAL PECULIARITIES OF BRUGADA SYNDROME AND ITS PHENOCOPIES
Abstract
The data of the examination, management, and long-term follow-up (21.2±8.4 months) of 6 patients aged 19 51 years from unrelated families with suspected Brugada syndrome are given.
About the Authors
A. Sh. Revishvili
Научный центр сердечно-сосудистой хирургии им. А.Н. Бакулева РАМН, г. Москва
Russian Federation
Russian Federation
I. V. Pronicheva
Научный центр сердечно-сосудистой хирургии им. А.Н. Бакулева РАМН, г. Москва
Russian Federation
Russian Federation
E. V. Zaklyazminskaya
ГУ Медико-генетический научный центр РАМН, г. Москва
Russian Federation
Russian Federation
E. A. Panteleeva
Научный центр сердечно-сосудистой хирургии им. А.Н. Бакулева РАМН, г. Москва
Russian Federation
Russian Federation
A. V. Polyakov
ГУ Медико-генетический научный центр РАМН, г. Москва
Russian Federation
Russian Federation
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Review
For citations:
Revishvili A.Sh., Pronicheva I.V., Zaklyazminskaya E.V., Panteleeva E.A., Polyakov A.V. MOLECULAR GENETIC AND CLINICAL PECULIARITIES OF BRUGADA SYNDROME AND ITS PHENOCOPIES. Journal of Arrhythmology. 2008;54(54):10-14. (In Russ.)
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