Article info
PDFOriginal article
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy
- Professor J A M Smeitink, Nijmegen Centre for Mitochondrial Disorders, Geert Grooteplein 10, PO Box 9101, 6500 HB Nijmegen, The Netherlands; j.smeitink{at}cukz.umcn.nl
Citation
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy
Publication history
- Received September 18, 2007
- Revised October 9, 2007
- Accepted October 10, 2007
- First published October 22, 2007.
Online issue publication
April 27, 2016
Article Versions
- 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
2008 BMJ Publishing Group