Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. (2010)

First Author: Zhou H
Attributed to:  MRC Centre for Neuromuscular Diseases in Children and Adults funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2009.12.005

PubMed Identifier: 20080402

Publication URI: http://europepmc.org/abstract/MED/20080402

Type: Journal Article/Review

Volume: 20

Parent Publication: Neuromuscular disorders : NMD

Issue: 3

ISSN: 0960-8966