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

被引：7

作者：

Blair, I. P. ^{[1
,2
]}

Vance, C. ^{[3
]}

Durnall, J. C. ^{[1
]}

Williams, K. L. ^{[1
]}

Thoeng, A. ^{[1
]}

Shaw, C. E. ^{[3
]}

Nicholson, G. A. ^{[1
,2
]}

机构：

[1] Concord Hosp, Northcott Neurosci Lab, ANZAC Res Inst, Sydney, NSW 2139, Australia

[2] Univ Sydney, Fac Med, Sydney, NSW 2006, Australia

[3] Kings Coll London, Sch Med, Dept Neurol, London WC2R 2LS, England

来源：

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY | 2008年 / 79卷 / 07期

基金：

英国医学研究理事会;

关键词：

D O I：

10.1136/jnnp.2007.140541

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：849 / 850

页数：4

共 5 条

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