King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene. (2011)

First Author: Dowling JJ

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2011.03.006

PubMed Identifier: 21514828

Publication URI: http://europepmc.org/abstract/MED/21514828

Type: Journal Article/Review

Volume: 21

Parent Publication: Neuromuscular disorders : NMD

Issue: 6

ISSN: 0960-8966