A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy. Issue 11 (16th October 2007) - Muglia, M; Vazza, G; Patitucci, A; Milani, M; Pareyson, D; Taroni, F; Quattrone, A; Mostacciuolo, M L