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. 2017 Oct 27;22(2):1350–1354. doi: 10.1111/jcmm.13409

Figure 1.

Figure 1

Clinical features of the patient with conduction diseases. (A) Symbols for affected individuals are coloured in. The proband (III‐2) was suffered from ventricular tachycardia, DCM and syncope. His mother (II‐3) and grandfather (I‐1) suddenly died with unknown reason. His uncle (II‐2) was also suffered from syncope for several times. (B) Electrocardiograms (ECGs) of the proband (III‐2). (C) Sanger DNA sequencing chromatogram demonstrates the heterozygosity for a GPD1L mutation (c.565C>T/p.Arg189*) in the proband and his uncle.