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:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


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Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 23714749

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Type: Journal Article/Review

Volume: 22

Parent Publication: European journal of human genetics : EJHG

Issue: 2

ISSN: 1018-4813