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

Baruteau, A-E; Kyndt, F; Behr, ER; Vink, AS; Lachaud, M; Joong, A; Schott, J-J; ... Probst, V; + view all Baruteau, A-E; Kyndt, F; Behr, ER; Vink, AS; Lachaud, M; Joong, A; Schott, J-J; Horie, M; Denjoy, I; Crotti, L; Shimizu, W; Bos, JM; Stephenson, EA; Wong, L; Abrams, DJ; Davis, AM; Winbo, A; Dubin, AM; Sanatani, S; Liberman, L; Kaski, JP; Rudic, B; Kwok, SY; Rieubland, C; Tfelt-Hansen, J; Van Hare, GF; Guyomarc'h-Delasalle, B; Blom, NA; Wijeyeratne, YD; Gourraud, J-B; Le Marec, H; Ozawa, J; Fressart, V; Lupoglazoff, J-M; Dagradi, F; Spazzolini, C; Aiba, T; Tester, DJ; Zahavich, LA; Beauséjour-Ladouceur, V; Jadhav, M; Skinner, JR; Franciosi, S; Krahn, AD; Abdelsayed, M; Ruben, PC; Yung, T-C; Ackerman, MJ; Wilde, AA; Schwartz, PJ; Probst, V; - view fewer (2018) SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups. European Heart Journal , 39 (31) pp. 2879-2887. 10.1093/eurheartj/ehy412 .

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