The A467T and W748SPOLG substitutions are a rare cause of adult-onset ataxia in Europe

被引：12

作者：

Craig, Kate

Ferrari, Gianfrancesco

Tiangyou, Watcharee

Hudson, Gavin

Gellera, Cinzia

Zeviani, Massimo

Chinnery, Patrick F.

机构：

[1] Univ Newcastle Upon Tyne, Mitochondrial Res Grp, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

[2] Univ Newcastle Upon Tyne, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

[3] Natl Neurol Inst, Unit Mol Neurogenet, Pierfranco & Luisa Mariani Ctr Study Childrens Mi, Milan, Italy

[4] Natl Neurol Inst, Div Biochem & Genet, Milan, Italy

来源：

BRAIN | 2007年 / 130卷

关键词：

D O I：

10.1093/brain/awm009

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页数：2

共 13 条

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