Article info
PDFMitochondrial disease
Original article
Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy
- Correspondence to Dr Shamima Rahman, Clinical and Molecular Genetics Unit, UCL Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK; s.rahman{at}ich.ucl.ac.uk
Citation
Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy
Publication history
- Received July 13, 2011
- Revised August 3, 2011
- Accepted August 11, 2011
- First published September 19, 2011.
Online issue publication
November 02, 2016
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Copyright information
© 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.