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- [2] A Novel KCNA1 Variant Manifesting as Persistent Limb Myokymia Without Episodic Ataxia JOURNAL OF CLINICAL NEUROLOGY, 2022, 18 (02): : 235 - 237
- [5] EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE KCNA1 (KV1.1) JOURNAL OF GENERAL PHYSIOLOGY, 1994, 104 (06): : A10 - A10
- [6] Case report: A novel loss-of-function pathogenic variant in the KCNA1 cytoplasmic N-terminus causing carbamazepine-responsive type 1 episodic ataxia FRONTIERS IN NEUROLOGY, 2022, 13
- [8] Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia Neurogenetics, 2007, 8 : 131 - 135
- [10] Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy MOLECULAR AND FUNCTIONAL DIVERSITY OF ION CHANNELS AND RECEPTORS, 1999, 868 : 442 - 446