Figure 1From: Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease shows a pedigree with novel mutations in connexin32. III-7, IV-4, IV-8, IV-12, IV-15 had the mutation c.225delG (R75fsX83) while IV-10, IV-14 and V-6 did not have the deletion.Back to article page