Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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author: Philippe Froguel, Beverley Balkau, Christian Dina, Jean-Jacques Schott, Hervé Le Marec, Stefan Kääb, Véronique Fressart, Florence Kyndt, Pascale Guicheney, Julien Barc, Pierre Lindenbaum, Stéphane Bézieau, Jacob Tfelt-Hansen, Antoine Leenhardt, Morten Salling Olesen, Richard Redon, Arie O. Verkerk, Tohru Minamino, Manfred Gessler, Ruben Coronel, Charles Antzelevitch, Peter J. Schwartz, Rachel Bastiaenen, Federica Dagradi, Lia Crotti, Vincent Probst, Elijah Behr, Martin Borggrefe, Rainer Schimpf, Dan Roden, Arthur Wilde, Eric Schulze-Bahr, Sven Zumhagen, Peter E Weeke, Connie R Bezzina, Seiko Ohno, Margherita Torchio, Wataru Shimizu, Minoru Horie, Naomasa Makita, Hanno Tan, Britt Maria Beckmann, Naoto Endo, Kanae Hasegawa, Stéphanie Chatel, Carol Ann Remme
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