Fig. 6From: 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 3. The proband, his mother, yonger maternal aunt and maternal grandfather who have pes cavus deformities have a c.103G > C (p.Val35Leu) hemizygous point mutation in the GJB1 geneBack to article page