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The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation—implications for diagnosis and management

Authors

  1. Correspondence to Dr Robert McFarland, Wellcome Trust Centre for Mitochondrial Research Group, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne NE2 4HH, UK; robert.mcfarland{at}ncl.ac.uk
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Citation

Nesbitt V, Pitceathly RDS, Turnbull DM, et al
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation—implications for diagnosis and management

Publication history

  • Received June 24, 2012
  • Revised December 24, 2012
  • Accepted December 26, 2012
  • First published January 25, 2013.
Online issue publication 
April 13, 2016

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