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Original article
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency

Authors

  1. Correspondence to Dr Grant A Mitchell, Division of Medical Genetics, CHU Sainte-Justine, 3175 Côte Sainte-Catherine, Montréal, Québec H3T 1C5, Canada; grant.mitchell{at}recherche-ste-justine.qc.ca
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Citation

Debray F, Morin C, Janvier A, et al
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency
Journal of Medical Genetics 2011;48:183-189.

Publication history

  • Received June 12, 2010
  • Revised September 28, 2010
  • Accepted September 29, 2010
  • First published January 25, 2011.
Online issue publication 
April 27, 2016

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© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.