Common and rare epilepsies share genetic determinants

被引：2
|
作者：
Striano, Pasquale [1 ]
Zara, Federico [2 ]
机构：
[1] Univ Genoa, Pediat Neurol & Muscular Dis Unit, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, G Gaslini Inst, Via Gaslini 5, I-16147 Genoa, Italy
[2] G Gaslini Inst Children, Lab Neurosci & Neurogenet, Dept Head & Neck Dis, Via Gaslini 5, I-16147 Genoa, Italy
来源：
NATURE REVIEWS NEUROLOGY | 2017年 / 13卷 / 04期
关键词：
D O I：
10.1038/nrneurol.2017.30
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
A whole-exome sequencing study has identified a series of ultra-rare variants that provide a genetic link between common and rare epilepsy syndromes. This discovery could open up new possibilities for personalized treatment of common epilepsies.
引用
收藏
页码：200 / 201
页数：2
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