The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease-Reference-Cited by-同舟云学术

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

Published:2015-11 Issue: Volume:25 Page:17-27
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Elson Joanna L.,Smith Paul M.,Greaves Laura C.,Lightowlers Robert N.,Chrzanowska-Lightowlers Zofia M.A.,Taylor Robert W.,Vila-Sanjurjo Antón

Funder

Marie Curie Actions programme of the European Commission

Wellcome Trust Centre for Mitochondrial Research

Medical Research Council (UK) Centre for Translational Muscle Disease Research

Medical Research Council (UK) Mitochondrial Disease Patient Cohort

Lily Foundation

UK NHS Highly Specialised “Rare Mitochondrial Disorders of Adults and Children” Service

Lifelong Health and Wellbeing

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

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5. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA;Andrews;Nat. Genet.,1999

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