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Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene. (2014)

First Author: Uusimaa J

Attributed to: Investigating the biology of mitochondrial DNA disease transmission to enable affected families to have healthy children 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