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Figure 1 | BMC Medical Genetics

Figure 1

From: Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3gene

Figure 1

Pedigrees of affected families: Open and black symbols represent unaffected and affected individuals, respectively. Dashed symbols indicate individuals with presumed or borderline disease phenotype. Grey symbols denote individuals with unknown clinical status. (+) and (-) symbols indicate presence and absence of the mutation, respectively. Index patients are marked by an arrow. Slanted bars denote deceased individuals.

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BMC Medical Genetics

ISSN: 1471-2350

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