Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation

被引：28

作者：

Dalpozzo, F

Rossetto, MG

Boaretto, F

Sartori, E

Mostacciuolo, ML

Daga, A

Bassi, MT

Martinuzzi, A

机构：

[1] Conegliano Res Ctr, E Medea Sci Inst, I-31015 Conegliano, TV, Italy

[2] Univ Padua, Dept Biol, I-35100 Padua, Italy

[3] Bosisio Parini Res Ctr, E Medea Sci Inst, Bosisio Parini, Italy

来源：

NEUROLOGY | 2003年 / 61卷 / 04期

关键词：

D O I：

10.1212/01.WNL.0000078189.73611.DF

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：580 / 581

页数：2

共 5 条

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[5] Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia [J].

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