Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT. (2013)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.mito.2013.03.002
PubMed Identifier: 23499752
Publication URI: http://europepmc.org/abstract/MED/23499752
Type: Journal Article/Review
Volume: 13
Parent Publication: Mitochondrion
Issue: 6
ISSN: 1567-7249