Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT. (2013)

First Author: Neeve VC
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


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Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 23499752

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Type: Journal Article/Review

Volume: 13

Parent Publication: Mitochondrion

Issue: 6

ISSN: 1567-7249