RT Journal Article
SR Electronic
T1 <em>CHMP2B</em> mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis
JF Journal of Neurology, Neurosurgery &amp; Psychiatry
JO J Neurol Neurosurg Psychiatry
FD BMJ Publishing Group Ltd
SP 849
OP 850
DO 10.1136/jnnp.2007.140541
VO 79
IS 7
A1 I P Blair
A1 C Vance
A1 J C Durnall
A1 K L Williams
A1 A Thoeng
A1 C E Shaw
A1 G A Nicholson
YR 2008
UL http://jnnp.bmj.com/content/79/7/849.abstract
AB