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pro vyhledávání: '"G Ribouleau"'
Autor:
V Probst, G Ribouleau, O Geoffroy, P Mabo, J Mansourati, J L Pasquie, D Babuty, A Al Arnaout, B Petit, O Billon, A Thollet, F Sacher, J B Gourraud
Publikováno v:
European Heart Journal. 43
Background Mutations in SCN5A are identified in approximately 20% to 30% of probands affected by Brugada syndrome (BrS). However, in familial studies, the relationship between SCN5A mutations and BrS remains poorly understood. The aim of this study w