Clinical and molecular analyses on two Japanese families with spinocerebellar ataxia type 23

被引：0
|
作者：
Kondo, Y. [1 ]
Miyazaki, D. [1 ]
Nakamura, K. [1 ]
Sato, S. [2 ]
Ohara, S. [3 ]
Yamaguchi, T. [4 ]
Ishikawa, M. [5 ]
Wakui, K. [4 ]
Kosho, T. [4 ]
Fukushima, Y. [4 ]
Sekijima, Y. [1 ]
Yoshida, K. [6 ]
机构：
[1] Shinshu Univ, Sch Med, Dept Med Neurol & Rheumatol, Matsumoto, Nagano, Japan
[2] Nagano Red Cross Hosp, Dept Neurol, Nagano, Japan
[3] Matsumoto Med Ctr, Dept Neurol, Matsumoto, Nagano, Japan
[4] Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano, Japan
[5] Shinshu Univ Hosp, Ctr Med Genet, Matsumoto, Nagano, Japan
[6] Shinshu Univ, Sch Med, Dept Brain Dis Res, Matsumoto, Nagano, Japan
来源：
JOURNAL OF THE NEUROLOGICAL SCIENCES | 2017年 / 381卷
关键词：
D O I：
10.1016/j.jns.2017.08.873
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
845
引用
收藏
页码：307 / 307
页数：1
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