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


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 26349026

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Type: Journal Article/Review

Parent Publication: Mitochondrion

ISSN: 1567-7249