Novel GRIN2B mutation: A rare cause of severe epileptic encephalopathy

被引：7
|
作者：
Sharawat, Indar Kumar [1 ]
Yadav, Jaivinder [1 ]
Saini, Lokesh [1 ]
机构：
[1] Postgrad Inst Med Educ & Res, Dept Pediat, Chandigarh, India
来源：
NEUROLOGY INDIA | 2019年 / 67卷 / 02期
关键词：
D O I：
10.4103/0028-3886.257986
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
引用
收藏
页码：562 / +
页数：2
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