A novel TSC2 mutation in a Korean patient with tuberous sclerosis complex

被引：0
|
作者：
Hu, Hae-Jin [1 ,2 ]
Chung, Yeun-Jun [1 ,2 ]
Yoo, Han-Wook [3 ,4 ]
Kim, Young-Hoon [5 ]
Eom, Tae-Hoon [5 ]
机构：
[1] Catholic Univ Korea, Dept Microbiol, Coll Med, Seoul 137701, South Korea
[2] Catholic Univ Korea, Integrated Res Ctr Genome Polymorphism, Coll Med, Seoul 137701, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pediat,Childrens Hosp, Seoul 138736, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Med Genet Ctr,Childrens Hosp, Seoul 138736, South Korea
[5] Catholic Univ Korea, Dept Pediat, Coll Med, Seoul 137701, South Korea
来源：
NEUROLOGICAL SCIENCES | 2014年 / 35卷 / 09期
关键词：
Tuberous Sclerosis Complex; Vigabatrin; Clinical Diagnostic Criterion; Cortical Tuber; Heterozygous Missense Mutation;
D O I：
10.1007/s10072-014-1803-8
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：1487 / 1489
页数：3
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