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The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease

Lookup NU author(s): Dr Joanna Elson, Dr Paul Smith, Professor Laura GreavesORCiD, Professor Robert Lightowlers, Professor Zofia Chrzanowska-LightowlersORCiD, Professor Robert Taylor

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).

Publication metadata

Author(s): Elson JL, Smith PM, Greaves LC, Lightowlers RN, Chrzanowska-Lightowlers ZMA, Taylor RW, Vila-Sanjurjo A

Publication type: Article

Publication status: Published

Journal: Mitochondrion

Year: 2015

Volume: 25

Pages: 17-27

Print publication date: 01/11/2015

Online publication date: 05/09/2015

Acceptance date: 27/08/2015

Date deposited: 08/09/2015

ISSN (print): 1567-7249

ISSN (electronic): 1872-8278

Publisher: Elsevier

URL: http://dx.doi.org/10.1016/j.mito.2015.08.004

DOI: 10.1016/j.mito.2015.08.004

PubMed id: 26349026

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Funding

Funder referenceFunder name
Lily Foundation
UK NHS Highly Specialised "Rare Mitochondrial Disorders of Adults and Children" Service
096919Z/11/ZWellcome Trust Centre for Mitochondrial Research
G0601943Medical Research Council (UK) Centre for Translational Muscle Disease Research
G0800674Medical Research Council (UK) Mitochondrial Disease Patient Cohort
MR/M501700cross-council Lifelong Health and Wellbeing initiative
PIIF-GA-2010-274660Marie Curie Actions programme of the European Commission
096919/Z/11/ZWellcome Trust

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