Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleThe E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.AuthorsMakita N; Behr E; Shimizu W; Horie M; Sunami A; Crotti L; Schulze-Bahr E; Fukuhara S; Mochizuki N; Makiyama T; Itoh H; Christiansen M; McKeown P; Miyamoto K; Kamakura S; Tsutsui H; Schwartz PJ; George AL Jr; Roden DMPublicationThe Journal of clinical investigation, 2008, Vol 118, Issue 6, p2219ISSN0021-9738Publication typearticleDOI10.1172/JCI34057