Outcomes and comorbidities of SCN1A-related seizure disorders
Author:
Funder
Stichting Vrienden WKZ
Stichting Panta Rhei
Dutch Epilepsy Foundation
COFRA
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Neurology (clinical),Neurology
Reference52 articles.
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2. SCN1A mutations and epilepsy;Mulley;Hum Mutat,2005
3. Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients;Depienne;J Med Genet,2009
4. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2;Escayg;Nat Genet,2000
5. Not all SCN1A epileptic encephalopathies are Dravet syndrome;Sadleir;Neurology,2017
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