Fig. 2From: A novel missense mutation in PLEKHG5 gene causing an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease in an Iraqi familySanger sequencing confirming homozygous c.1844C > A mutation in the patient (A) and heterozygous mutation in his parents (B, C). D Diagram structure of PLEKHG5 protein. Schematic of PLEKHG5 protein shows the locations of the pathogenic variant in humansBack to article page