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Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome
  1. Correspondence to Dr H J M Smeets, Department of Genetics and Cell Biology, PO Box 616, 6200 MD Maastricht, the Netherlands; Bert.Smeets{at}molcelb.unimaas.nl
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Citation

Gerards M, Sluiter W, van den Bosch BJC, et al
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

Publication history

  • Received March 5, 2009
  • Revised May 19, 2009
  • Accepted May 25, 2009
  • First published June 18, 2009.
Online issue publication 
July 23, 2010

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