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Figure 2 | BMC Medical Genetics

Figure 2

From: Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy

Figure 2

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.

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