Mutation analysis of PMP22 in Slovak patientswith Charcot-Marie-Toothdisease and hereditary neuropathy with liability to pressure palsies.
All authors: Resko P, Radvansky J, Odnogova Z, Baldovic M, Minarik G, Polakova H, Palffy R, Kadasy L
General Physiology and Biophysics, 30 (4): 379-388, 2011