SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

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Published in:Archives of cardiovascular diseases supplements 2019-09, Vol.11 (4), p.e381-e382
Main Authors: Baruteau, Alban-Elouen, Kyndt, Florence, Behr, Elijah, Vink, Arja, Lachaud, Matthias, Joong, Anna, Schott, Jean-Jacques, Horie, Minoru, Denjoy, Isabelle, Crotti, Lia, Shimizu, Wataru, Bos, Johan, Stephenson, Elizabeth, Wong, Leonie, Abrams, Dominic, Davis, Andrew, Winbo, Annika, Dubin, Anne, Sanatani, Shubhayan, Liberman, Leonardo, Kaski, Juan-Pablo, Rudic, Boris, Kwok, Sit Yee, Rieubland, Claudine, Tfelt-Hansen, Jacob, Van Hare, George, Guyomarc’h-Delasalle, Béatrice, Blom, Nico, Wijeyeratne, Yanushi, Gourraud, Jean-Baptiste, Le Marec, Hervé, Ozawa, Junichi, Fressart, Véronique, Lupoglazoff, Jean-Marc, Dagradi, Federica, Spazzolini, Carla, Aiba, Takeshi, Tester, David, Zahavich, Laura, Beauséjour-Ladouceur, Virginie, Jadhav, Mangesh, Skinner, Jonathan, Franciosi, Sonia, Krahn, Andrew, Abdelsayed, Mena, Ruben, Peter, Yung, Tak-Cheung, Ackerman, Michael, Wilde, Arthur, Schwartz, Peter, Probst, Vincent
Format: Article
Language:English
Online Access:Get full text
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ISSN:1878-6480
DOI:10.1016/j.acvdsp.2019.06.005