RYR1 mutations are a common cause of congenital myopathies with central nuclei. (2010)

First Author: Wilmshurst JM

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/ana.22119

PubMed Identifier: 20839240

Publication URI: http://europepmc.org/abstract/MED/20839240

Type: Journal Article/Review

Volume: 68

Parent Publication: Annals of neurology

Issue: 5

ISSN: 0364-5134