Fig. 1: Family pedigree charts of patients with the DSG2 (c.355 C > T, p.Arg119Ter) variant. | Human Genome Variation

Fig. 1: Family pedigree charts of patients with the DSG2 (c.355 C > T, p.Arg119Ter) variant.

From: Four cardiomyopathy patients with a heterozygous DSG2 p.Arg119Ter variant

Fig. 1: Family pedigree charts of patients with the DSG2 (c.355 C > T, p.Arg119Ter) variant.

The black arrows indicate Pt-1 (III-3), Pt-2 (II-4), Pt-3 (II-1), and Pt-4 (II-1). A family history of cardiovascular diseases or abnormal findings on cardiovascular examination (indicated as black squares or circles) was observed in Pt-1 (I-1: sudden death at 73 y; I-2: pacemaker implantation; II-2: enlarged heart on chest X-ray) but not in Pt-2, 3, or 4.

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