Article info
PDFLetter
CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis
- Dr I P Blair, Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord Hospital NSW 2139, Australia; iblair{at}med.usyd.edu.au
Citation
CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis
Publication history
- First published February 12, 2008.
Online issue publication
June 16, 2008
Article Versions
- Previous version (12 February 2008).
- 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