S151A d-sarcoglycan mutation causes a mild phenotype of cardiomyopathy in mice. (2014)

First Author: Rutschow D
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


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