Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene. (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.2013.112
PubMed Identifier: 23714749
Publication URI: http://europepmc.org/abstract/MED/23714749
Type: Journal Article/Review
Volume: 22
Parent Publication: European journal of human genetics : EJHG
Issue: 2
ISSN: 1018-4813