A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene. (2013)
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/s00415-012-6817-7
PubMed Identifier: 23329375
Publication URI: http://europepmc.org/abstract/MED/23329375
Type: Journal Article/Review
Volume: 260
Parent Publication: Journal of neurology
Issue: 6
ISSN: 0340-5354