The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.

Makita, N; Behr, E; Shimizu, W; Horie, M; Sunami, A; Crotti, Lia; Schulze Bahr, E; Fukuhara, S; Mochizuki, N; Makiyama, T; Itoh, H; Christiansen, M; Mckeown, P; Miyamoto, K; Kamakura, S; Tsutsui, H; Schwartz, Peter; George AL, Jr; Roden, Dm