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Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome
- 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
Citation
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 29, 2016
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Web Only Data jmg.2009.067553
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© 2009, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.