Palmoplantar keratoderma and Charcot–Marie–Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole‐exome sequencing. (1st July 2017) - Gagliardi, S.; Ricca, I.; Ferrarini, A.; Valente, M.; Grieco, G.S.; Piccolo, G.; Alfonsi, E.; Delledonne, M.; Cereda, C.