The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease. (2015)
Attributed to:
Centre for Ageing and Vitality
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.mito.2015.08.004
PubMed Identifier: 26349026
Publication URI: http://europepmc.org/abstract/MED/26349026
Type: Journal Article/Review
Volume: 25
Parent Publication: Mitochondrion
ISSN: 1567-7249