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