SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups
- Resource Type
- Abstract
- 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
- Source
- In Archives of Cardiovascular Diseases Supplements September 2019 11(4):e381-e382
- Subject
- Language
- ISSN
- 1878-6480