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Original article
Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency

Authors

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

Jackson CB, Nuoffer J, Hahn D, et al
Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency

Publication history

  • Received July 18, 2013
  • Revised November 21, 2013
  • Accepted November 27, 2013
  • First published December 23, 2013.
Online issue publication 
February 14, 2014

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