PMP2 and Charcot-Marie-Tooth disease: Here, we report clinical and electrophysiological data from all the members of three generations of a CMT family harboring a heterozygous deletion c.147_149delTAT in the PMP2 gene, which leads to an isoleucine loss at codon 50 (p.Ile50del) that segregates with the disease, as previously described in the literature by Gerlodi et al. [10].