ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy. (2013)

First Author: Haack TB
Attributed to:  Mitochondrial Genetics funded by MRC


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