Fig. 2From: Recurrent episodes of reversible posterior leukoencephalopathy in three Chinese families with GJB1 mutations in X-linked Charcot-Marie-tooth type 1 disease: cases reportPedigree of Family 1. The proband, his mother, older maternal aunt and her daughter as well as younger maternal aunt who have pes cavus deformities have a c.425G > A (p.Arg142Glu) hemizygous point mutation in the GJB1 geneBack to article page