共 50 条
- [3] Gain-of-function mutation Met136Val in SCN8A may not be a common cause of trigeminal neuralgia MOLECULAR GENETICS & GENOMIC MEDICINE, 2021, 9 (02):
- [6] Novel epilepsy phenotype associated to a known SCN8A mutation SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2019, 67 : 15 - 17
- [7] SCN8A epileptic encephalopathy mutations display a gain-of-function phenotype and divergent sensitivity to antiepileptic drugs Acta Pharmacologica Sinica, 2022, 43 : 3139 - 3148