Article info
PDFShort report
A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy
- Correspondence to Dr C Geoffrey Woods, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, UK; cw347{at}cam.ac.ukand Lihadh Al-Gazali Department of Pediatrics, Faculty of Medicine & Health Sciences, United Arab Emirates University, United Arab Emirates; algazali{at}hotmail.com
Citation
A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy
Publication history
- Received May 21, 2010
- Revised July 9, 2010
- Accepted July 27, 2010
- First published October 26, 2010.
Online issue publication
January 27, 2011
Article Versions
- Previous version (26 October 2010).
- You are viewing the most recent version of this article.
Web Only Data
Files in this Data Supplement:
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. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.