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A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene. (2013)

First Author: Løseth S

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