S151A d-sarcoglycan mutation causes a mild phenotype of cardiomyopathy in mice. (2014)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2013.97
PubMed Identifier: 23695275
Publication URI: http://europepmc.org/abstract/MED/23695275
Type: Journal Article/Review
Volume: 22
Parent Publication: European journal of human genetics : EJHG
Issue: 1
ISSN: 1018-4813