| 1 | EIEE52, SCN1B |
| Do mutations in SCN1B cause Dravet syndrome? | |
| Kim YO, Dibbens L, Marini C, Suls A, Chemaly N, Mei D, McMahon JM, Iona X, Berkovic SF, De Jonghe P, Guerrini R, Nabbout R, Scheffer IE. | |
| Epilepsy Res 103(1):97-100. doi: 10.1016/j.eplepsyres.2012.10.009. Epub 2012 Nov 20. 2013 | |
| 2 | EIEE52, SCN1B |
| A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome. | |
| Ogiwara I, Nakayama T, Yamagata T, Ohtani H, Mazaki E, Tsuchiya S, Inoue Y, Yamakawa K. | |
| Epilepsia 53(12):e200-3. doi: 10.1111/epi.12040. Epub 2012 Nov 13. 2012 | |