1. A cohort study of MFN2 mutations and phenotypic spectrums in Charcot–Marie–Tooth disease 2A patients. (18th June 2014) Authors: Choi, B.‐O.; Nakhro, K.; Park, H.J.; Hyun, Y.S.; Lee, J.H.; Kanwal, S.; Jung, S.‐C.; Chung, K.W. Journal: Clinical genetics Issue: Volume 87:Number 6(2015:Jun.) Page Start: 594 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗