Article info
Letter
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
April 13, 2016
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2008 BMJ Publishing Group