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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2

Fig. 2

Pedigrees of the two families affected with the c.1003A > G, p.(Thr335Ala) mutation in DSG2. Black-filled symbols represent individuals who fulfill the 2010 Task Force Criteria by Marcus et al. [9]. Age of the family members and their genotypes are listed below the symbols. Parents of the affected individuals in family 1 are obligatory carriers of the variant. In family 2, one of them is an obligatory heterozygous carrier, while the other may either be heterozygous or homozygous for the variant

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BMC Medical Genetics

ISSN: 1471-2350

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