Article info
PDFMitochondrial disease
Original article
Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
- Correspondence to Professor Jo Poulton, Nuffield Department of Obstetrics and Gynaecology, The Women's Centre, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK; joanna.poulton{at}obs-gyn.ox.ac.uk
Citation
Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
Publication history
- Received February 7, 2011
- Revised April 4, 2011
- Accepted April 5, 2011
- First published September 19, 2011.
Online issue publication
September 19, 2011
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
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.