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

Alban Elouen Baruteau, Florence Kyndt, Elijah R. Behr, Arja S. Vink, Matthias Lachaud, Anna Joong, Jean Jacques Schott, Minoru Horie, Isabelle Denjoy, Lia Crotti, Wataru Shimizu, Johan M. Bos, Elizabeth A. Stephenson, Leonie Wong, Dominic J. Abrams, Andrew M. Davis, Annika Winbo, Anne M. Dubin, Shubhayan Sanatani, Leonardo LibermanJuan Pablo Kaski, Boris Rudic, Sit Yee Kwok, Claudine Rieubland, Jacob Tfelt-Hansen, George F. Van Hare, Béatrice Guyomarc'h-Delasalle, Nico A. Blom, Yanushi D. Wijeyeratne, Jean Baptiste Gourraud, Hervé Le Marec, Junichi Ozawa, Véronique Fressart, Jean Marc Lupoglazoff, Federica Dagradi, Carla Spazzolini, Takeshi Aiba, David J. Tester, Laura A. Zahavich, Virginie Beauséjour-Ladouceur, Mangesh Jadhav, Jonathan R. Skinner, Sonia Franciosi, Andrew D. Krahn, Mena Abdelsayed, Peter C. Ruben, Tak Cheung Yung, Michael J. Ackerman, Arthur A. Wilde, Peter J. Schwartz, Vincent Probst

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