De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies
| Date first appeared online | 28/07/2016 |
| DOI | 10.1016/j.ajhg.2016.06.003 |
| Authors | Pickrell O., Chung S., Rees M. |
| Journal Name | The American Journal of Human Genetics |
| Volume | 99 |
Documents
- Epi4K_AJHG_D_16_00171_R2_FINAL_23may2016v2.pdf , Book, Released under the terms of a Creative Commons Attribution Non-Commercial No Derivatives License (CC-BY-NC-ND).