Citations for
1EIEE62, SCN3A
Mutations in SCN3A cause early infantile epileptic encephalopathy.
Zaman T, Helbig I, Božović IB, DeBrosse SD, Bergqvist AC, Wallis K, Medne L, Maver A, Peterlin B, Helbig KL, Zhang X, Goldberg EM.
Ann Neurol 83(4):703-717. doi: 10.1002/ana.25188. Epub 2018 Mar 30. 2018
2EIEE62, SCN2A, SCN3A
Deletions of SCN2A and SCN3A genes in a patient with West syndrome and autistic spectrum disorder.
Chong PF, Saitsu H, Sakai Y, Imagi T, Nakamura R, Matsukura M, Matsumoto N, Kira R.
Seizure 60:91-93. doi: 10.1016/j.seizure.2018.06.012. Epub 2018 Jun 13. 2018