Fig. 1From: Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from IsraelFamily pedigree and c.103G > T co-segregation. Extended family pedigree of the Israeli family investigated with genotypes showing the presence or absence of GAN c.103G > T in affected and unaffected subjects respectively, who have been included in this studyBack to article page