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Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition
  1. Correspondence to:
 Dr Peter J Bridge
 Molecular Diagnostic Laboratory, Alberta Children’s Hospital, 1820 Richmond Road SW, Calgary, Alberta T2T 5C7, Canada; peter.bridge{at}calgaryhealthregion.ca
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Citation

Davey KM, Parboosingh JS, McLeod DR, et al
Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

Publication history

  • Received July 5, 2005
  • Accepted July 26, 2005
  • Revised July 5, 2005
  • First published July 31, 2005.
Online issue publication 
April 28, 2006

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