DEPDC5 mutations in familial and sporadic focal epilepsy

Background and Aims: Mutations in the disheveled, Egl-10 and pleckstrin domain-containing protein 5 (DEPDC5) gene have emerged as an important cause of various familial focal epilepsy syndromes. However, the significance of DEPDC5 mutations in patients with sporadic focal epilepsy has yet to be char...

Full description

Saved in:
Bibliographic Details
Main Authors: Tsai, Meng Han, Chan, Chung Kin, Chang, Ying Chao, Yu, Y.T., Chuang, S.T., Fan, W.L., Ling, S.C., Fu, Ting Ying, Chang, Wen Neng, Liou, Chia Wei, Chuang, Yao Chung, Ng, Ching Ching, Hwang, Daw Yang, Lim, Kheng Seang
Format: Article
Published: Wiley 2017
Subjects:
Online Access:http://eprints.um.edu.my/22872/
https://doi.org/10.1111/cge.12992
Tags: Add Tag
No Tags, Be the first to tag this record!