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)

First Author: Elson J
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.2015.08.004

PubMed Identifier: 26349026

Publication URI: http://europepmc.org/abstract/MED/26349026

Type: Journal Article/Review

Parent Publication: Mitochondrion

ISSN: 1567-7249