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6. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases. Six I, Hermida JS, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P. Europace; 2008 Jan 01; 10(1):79-85. PubMed ID: 18156160 [Abstract] [Full Text] [Related]
19. Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome. Santos LF, Rodrigues B, Moreira D, Correia E, Nunes L, Costa A, Elvas L, Pereira T, Machado JC, Castedo S, Henriques C, Matos A, Santos JO. Europace; 2012 Jun 15; 14(6):882-8. PubMed ID: 22277643 [Abstract] [Full Text] [Related]