共 6 条
A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation
被引:1
作者:

Vercammen, Johanna
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机构:
Univ Hosp Leuven, Dept Neurol, Leuven, Belgium Univ Hosp Leuven, Dept Neurol, Leuven, Belgium

Terryn, Joke
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h-index: 0
机构:
Univ Hosp Leuven, Dept Neurol, Leuven, Belgium Univ Hosp Leuven, Dept Neurol, Leuven, Belgium

Van Daele, Sien
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机构:
Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium Univ Hosp Leuven, Dept Neurol, Leuven, Belgium

Vermeer, Sascha
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机构:
Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium Univ Hosp Leuven, Dept Neurol, Leuven, Belgium

Vandenberghe, Wim
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机构:
Univ Hosp Leuven, Dept Neurol, Leuven, Belgium
Katholieke Univ Leuven, Dept Neurosci, Leuven, Belgium
Univ Hosp Leuven, Dept Neurol, Herestr 49, B-3000 Leuven, Belgium Univ Hosp Leuven, Dept Neurol, Leuven, Belgium
机构:
[1] Univ Hosp Leuven, Dept Neurol, Leuven, Belgium
[2] Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium
[3] Katholieke Univ Leuven, Dept Neurosci, Leuven, Belgium
[4] Univ Hosp Leuven, Dept Neurol, Herestr 49, B-3000 Leuven, Belgium
关键词:
benign hereditary chorea;
TITF1;
TITF-1;
Huntington's disease;
saccadic;
D O I:
10.1002/mdc3.14013
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
收藏
页码:738 / 741
页数:4
相关论文
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