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Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome
- Correspondence to Dr Elsebet Ostergaard, Department of Clinical Genetics 4062, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, Copenhagen 2100, Denmark; elsebet.ostergaard{at}dadlnet.dk
Citation
Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome
Publication history
- Received January 10, 2011
- Revised April 7, 2011
- Accepted April 18, 2011
- First published May 26, 2011.
Online issue publication
April 28, 2021
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© 2011, 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.