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Letter
CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis

Authors

  1. Dr I P Blair, Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord Hospital NSW 2139, Australia; iblair{at}med.usyd.edu.au
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Citation

Blair IP, Vance C, Durnall JC, et al
CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis
Journal of Neurology, Neurosurgery & Psychiatry 2008;79:849-850.

Publication history

  • First published February 12, 2008.
Online issue publication 
April 13, 2016

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2008 BMJ Publishing Group