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- W4319950007 abstract "PRRT2 is located on chromosome 16p11.2 and is a transmembrane protein highly expressed in the CNS that has been identified to play a role in epilepsy, movement disorders and hemiplegic migraines. Specifically, variants are identified in families with paroxysmal kinesigenic dyskinesia." @default.
- W4319950007 created "2023-02-11" @default.
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- W4319950007 creator A5017883444 @default.
- W4319950007 date "2022-12-31" @default.
- W4319950007 modified "2023-09-26" @default.
- W4319950007 title "Treatment of Bi-Allelic PRRT-2 Mutation Associated Ataxia and Paroxysmal Dyskinesia" @default.
- W4319950007 doi "https://doi.org/10.36959/595/442" @default.
- W4319950007 hasPublicationYear "2022" @default.
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