P1799Identification of a novel gene mutation in TRPM4 in a family with premature SCD, cardiac conduction disease and cardiomyopathy. (28th August 2018) - Winnik, S; Medeiros-Domingo, A; Biskup, S; Breitenstein, A; Brunckhorst, C; Steffel, J; Ruschitzka, F; Duru, F; Saguner, A