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...
| Main Authors: | , , , , , , , , , , , , , |
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| Format: | Article |
| Published: |
Wiley
2017
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| Subjects: |