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The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online

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Description scientific article published in May 2007
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author: Gisela M Terwindt  Joost Haan  Kaate R J Vanmolkot  Martin Dichgans  Michael Pusch  Michel Ferrari  Anine H Stam 

Publication date May 1, 2007
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