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Short report
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation

Authors

  1. Correspondence to Dr Ronen Spiegel, Department of Pediatrics B, Emek Medical Center, Afula 18101, Israel; spiegelr{at}zahav.net.il, spiegel_ro{at}clalit.org.il
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Citation

Spiegel R, Saada A, Flannery PJ, et al
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation

Publication history

  • Received July 5, 2015
  • Revised August 10, 2015
  • Accepted August 11, 2015
  • First published November 11, 2015.
Online issue publication 
January 21, 2016

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