ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy. (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/10.1016/j.ajhg.2013.06.006
PubMed Identifier: 23849775
Publication URI: http://europepmc.org/abstract/MED/23849775
Type: Journal Article/Review
Volume: 93
Parent Publication: American journal of human genetics
Issue: 2
ISSN: 0002-9297