Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes
No Thumbnail Available
Date
2011
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
Description
Keywords
ARCMT, CMT4B1, CMT4F, MTMR2 and PRX genes, Vocal cord palsy, Skeletal deformities