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Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease
- Correspondence to: Dr M J Blok Department of Clinical Genetics, University Hospital, PO Box 5800, 6202 AZ Maastricht, The Netherlands; rien.blok{at}gen.unimaas.nl
Citation
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease
Publication history
- Received August 4, 2006
- Accepted January 19, 2007
- Revised January 17, 2007
- First published March 30, 2007.
Online issue publication
April 27, 2016
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Copyright 2007 Journal of Medical Genetics