共 50 条
- [33] Variable K+ channel subunit dysfunction in inherited mutations of KCNA1 JOURNAL OF PHYSIOLOGY-LONDON, 2002, 538 (01): : 5 - 23
- [34] Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentations neurogenetics, 2016, 17 : 11 - 16
- [40] Episodic ataxia type 2 (EA2) with interictal myokymia and focal dystonia COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2022, 8 (06):