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Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy

RepositoryUniversity of Melbourne [Minerva Access]
URLhttp://hdl.handle.net/11343/213182
Author(s)orcid:0000-0003-1949-8489; orcid:0000-0001-5132-0774; orcid:0000-0003-4580-841X; orcid:0000-0002-2311-2174; orcid:0000-0002-7884-6861; Corbett, MA; Bellows, ST; Li, M; Carroll, R; Micallef, S; Carvill, GL; Myers, CT; Howell, KB; Maljevic, S; Lerche, H; Ga
Item typeArticle
JournalNeurology, Print_ISSN:0028-3878, Online_ISSN:1526-632X
DOIhttps://doi.org/10.1212/WNL.0000000000003309

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