Fig. 4From: 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 2. The proband has a c.563 C > T (p.Thr188Ile) hemizygous point mutation in the GJB1 geneBack to article page