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Published in 2021 at "Frontiers in Neurology"
DOI: 10.3389/fneur.2021.703970
Abstract: Introduction: Among genetic paroxysmal movement disorders, variants in ion channel coding genes constitute a major subgroup. Loss-of-function (LOF) variants in KCNA1, the gene coding for KV1.1 channels, are associated with episodic ataxia type 1 (EA1),…
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Keywords:
episodic ataxia;
treatment;
associated episodic;
sodium channel ... See more keywords