SCN2A- Associated Episodic and Persistent Ataxia with Cerebellar Atrophy: A Case Report
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SCN2A, a gene that codes for a sodium channel highly expressed in the cerebellum, has been linked to a heterogeneous phenotype, including episodic ataxia (EA) and epilepsy, among other symptoms1. Given the rarity of SCN2A-associated EA and its recent descripti... ...
