Article info
PDFPostScript
Correspondence
Leigh disease due to SCO2 mutations revealed at extended autopsy
- Correspondence to Dr Katarzyna Iwanicka-Pronicka, Department of Audiology and Phoniatrics, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, Warszawa 04-730, Poland; katarzynapronicka{at}gmail.com
Citation
Leigh disease due to SCO2 mutations revealed at extended autopsy
Publication history
- Received September 15, 2014
- Revised December 31, 2014
- Accepted January 18, 2015
- First published February 26, 2015.
Online issue publication
April 18, 2016
Article Versions
- Previous version (18 April 2016).
- You are viewing the most recent version of this article.
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
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