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Novel mitochondrial tRNAIle m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype

Authors

  1. Correspondence to Dr André Schaller, Division of Human Genetics, Departments of Pediatrics and Clinical Research, Inselspital, University of Berne, Freiburgstrasse, Berne CH-3010, Switzerland andre.schaller{at}insel.ch
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Citation

Jackson CB, Neuwirth C, Hahn D, et al
Novel mitochondrial tRNAIle m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype

Publication history

  • Received March 25, 2014
  • Revised June 12, 2014
  • Accepted June 22, 2014
  • First published July 17, 2014.
Online issue publication 
September 16, 2014

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