RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling. (2013)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.22326
PubMed Identifier: 23553787
Publication URI: http://europepmc.org/abstract/MED/23553787
Type: Journal Article/Review
Volume: 34
Parent Publication: Human mutation
Issue: 7
ISSN: 1059-7794