Mutation analysis of PMP22 in Slovak patientswith Charcot-Marie-Toothdisease and hereditary neuropathy with liability to pressure palsies.
Our authors: Minárik Gabriel
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

https://www.ncbi.nlm.nih.gov/pubmed/22131320