Fig. 2From: Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from IsraelProtein homology of GAN in various species and the p.Val35Phe mutant molecule. The mutation results in an amino acid substitution at Valine (indicated by the red box) to phenylalanine at position 35, a residue highly conserved across speciesBack to article page