DEPDC5 mutations in familial and sporadic focal epilepsy

• 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: QH Natural history; R Medicine
• Online Access: http://eprints.um.edu.my/22872/; https://doi.org/10.1111/cge.12992

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...