Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. (2009)

First Author: Jungbluth H

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2009.02.005

PubMed Identifier: 19303294

Publication URI: http://europepmc.org/abstract/MED/19303294

Type: Journal Article/Review

Volume: 19

Parent Publication: Neuromuscular disorders : NMD

Issue: 5

ISSN: 0960-8966