Analysis of NIPA1 (SPG6) mutations in autosomal dominant spastic paraplegia

被引：0
|
作者：
Klebe, S.
Lacour, A.
Durr, A.
Stojkovic, T.
Depienne, C.
Forlani, S.
Dussert, C.
Poea-Guyon, S.
Vuillaume, I.
Sablonniere, B.
Vermersch, P.
Brice, A.
Stevanin, G.
机构：
来源：
MOVEMENT DISORDERS | 2006年 / 21卷
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暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P294
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页码：S409 / S409
页数：1
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