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- [21] 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
- [23] Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disorders MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (10):
- [24] Interictal Headache, Pseudodystonia, and Persistent Ataxia in Episodic Ataxia Type 1 Due to a Novel KCNA1 Gene Mutation MOVEMENT DISORDERS CLINICAL PRACTICE, 2022, 9 (02): : 272 - 274
- [26] Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia Neurogenetics, 2007, 8 : 131 - 135
- [28] Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function FASEB JOURNAL, 1999, 13 (11): : 1335 - 1345