Scn5a mutation type and a genetic risk score associate variably with brugada syndrome phenotype in scn5a families

Yanushi D. Wijeyeratne, Michael W. Tanck, Yuka Mizusawa, Velislav Batchvarov, Julien Barc, Lia Crotti, J. Martijn Bos, David J. Tester, Alison Muir, Christian Veltmann, Seiko Ohno, Stephen P. Page, Joseph Galvin, Rafik Tadros, Martina Muggenthaler, Hariharan Raju, Isabelle Denjoy, Jean Jacques Schott, Jean Baptiste Gourraud, Doris Skoric-MilosavljevicEline A. Nannenberg, Richard Redon, Michael Papadakis, Florence Kyndt, Federica Dagradi, Silvia Castelletti, Margherita Torchio, Thomas Meitinger, Peter Lichtner, Taisuke Ishikawa, Arthur A.M. Wilde, Kazuhiro Takahashi, Sanjay Sharma, Dan M. Roden, Martin M. Borggrefe, Pascal P. McKeown, Wataru Shimizu, Minoru Horie, Naomasa Makita, Takeshi Aiba, Michael J. Ackerman, Peter J. Schwartz, Vincent Probst, Connie R. Bezzina, Elijah R. Behr

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