Article info
PDFOriginal article
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome
- Correspondence to Dr Ronen Spiegel, Paediatric Department A' and Genetic Institute Ha'Emek Medical Center, Afula, Israel; spiegelr{at}zahav.net.il
Citation
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome
Publication history
- Received August 30, 2010
- Revised September 22, 2010
- Accepted September 28, 2010
- First published December 8, 2010.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
- Previous version (27 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
© 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.