Figure 2From: Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy Pedigrees with the electropherogram of the frameshift and intronic mutations. Squares are males and circles are females. Filled in black are cases with HCM. Symbols with a black vertical bar represent relatives that were considered possibly affected. N means normal phenotype, empty symbols are non-evaluated relatives. The arrows indicate the index patients. Diagonal lines indicate deceased individual. + indicate carriers of the mutation and - indicates the non-carriers. SD means sudden death.Back to article page