共 50 条
- [21] Three novel KCNA1 mutations in episodic ataxia type I families Human Genetics, 1998, 102 : 464 - 466
- [23] A Novel KCNA1 Variant Manifesting as Persistent Limb Myokymia Without Episodic Ataxia JOURNAL OF CLINICAL NEUROLOGY, 2022, 18 (02): : 235 - 237
- [25] Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia Neurogenetics, 2007, 8 : 131 - 135
- [27] Episodic ataxia type 1 without episodic ataxia: the diagnostic utility of nerve excitability studies in individuals with KCNA1 mutations DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2013, 55 (10): : 959 - 962
- [28] Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene FRONTIERS IN PHYSIOLOGY, 2015, 5