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PDFOriginal article
Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition
- 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
Citation
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 27, 2016
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Copyright 2006 Journal of Medical Genetics