Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes

被引：6
作者：
Brugman, Frans [1 ]
Scheffer, Hans [3 ]
Schelhaas, H. Jurgen [2 ]
Nillesen, Willy M. [3 ]
Wokke, John H. J. [1 ]
van de Warrenburg, Bart P. C. [1 ,2 ]
van den Berg, Leonard H.
机构：
[1] Univ Med Ctr Utrecht, Rudolf Magnus Inst Neurosci, Dept Neurol, NL-3508 GA Utrecht, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Donders Ctr Neurosci, Dept Neurol, NL-6525 ED Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 ED Nijmegen, Netherlands
来源：
JOURNAL OF NEUROLOGY | 2009年 / 256卷 / 05期
关键词：
HEREDITARY SPASTIC PARAPLEGIA; AMYOTROPHIC-LATERAL-SCLEROSIS; SILVER-SYNDROME; CLINICAL-FEATURES; NEUROPATHY; FAMILIES; CRITERIA; BSCL2;
D O I：
10.1007/s00415-009-5009-6
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：824 / 826
页数：3
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