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. Author manuscript; available in PMC: 2018 Aug 3.
Published in final edited form as: JACC Clin Electrophysiol. 2018 Feb 2;4(4):504–514. doi: 10.1016/j.jacep.2017.12.003

FIGURE 1. Pedigrees of DCM Families With FLNC Truncating Variants Displaying an Arrhythmogenic Phenotype.

FIGURE 1

(A) Squares indicate males, circles indicate females, slashes indicate deceased individuals, black shading indicates a dilated cardiomyopathy (DCM) phenotype, and vertical lines indicate history of heart disease. The arrows indicate the proband. Carriers (+) and noncarriers (−) of a FLNC truncation variant are shown. (B) Electrocardiogram of subject TSSDC130 (II:3) shows sustained ventricular tachycardia. (C) Electrocardiogram depicts nonsustained ventricular tachycardia from individual II:1 (family DNFDC057) (9).