Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation. (2015)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00415-015-7800-x
PubMed Identifier: 26048687
Publication URI: http://europepmc.org/abstract/MED/26048687
Type: Journal Article/Review
Volume: 262
Parent Publication: Journal of neurology
Issue: 8
ISSN: 0340-5354