CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis.
Blair, I. P.; Vance, C.; Durnall, J. C.; Williams, K. L.; Thoeng, A.; Shaw, C. E.; Nicholson, G. A.; Journal of Neurology, Neurosurgery & Psychiatry, 2008, vol. 79, issue 7, p 849, ISSN 00223050. ISBN 1468330x.

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