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- [2] Three novel KCNA1 mutations in episodic ataxia type I families Human Genetics, 1998, 102 : 464 - 466
- [4] A Novel KCNA1 Variant Manifesting as Persistent Limb Myokymia Without Episodic Ataxia JOURNAL OF CLINICAL NEUROLOGY, 2022, 18 (02): : 235 - 237
- [7] 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
- [8] 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