CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis. Issue 7 (12th February 2008)

Record Type:: Journal Article
Title:: CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis. Issue 7 (12th February 2008)
Main Title:: CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis
Authors:: Blair, I P
Vance, C
Durnall, J C
Williams, K L
Thoeng, A
Shaw, C E
Nicholson, G A
Abstract:
Is Part Of:: Journal of neurology, neurosurgery and psychiatry. Volume 79:Issue 7(2008)
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 79:Issue 7(2008)
Issue Display:: Volume 79, Issue 7 (2008)
Year:: 2008
Volume:: 79
Issue:: 7
Issue Sort Value:: 2008-0079-0007-0000
Page Start:: 849
Page End:: 850
Publication Date:: 2008-02-12
Subjects:: Neurology -- Periodicals
Nervous system -- Surgery -- Periodicals
Psychiatry -- Periodicals
616.8
Journal URLs:: http://jnnp.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?action=archive&journal=192 ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jnnp.2007.140541 ↗
Languages:: English
ISSNs:: 0022-3050
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 18271.xml