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SCN1A
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Zebrafish larvae with Scn1a (Nav1.1) mutation
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SCN1A as a therapeutic target for Dravet syndrome.
SCN1A: bioinformatically informed revised boundaries for promoter and enhancer regions.
Ictal vocalizations in the Scn1a+/- mouse model of Dravet syndrome.
Idealized multiple-timescale model of cortical spreading depolarization initiation and pre-epileptic…
Dravet syndrome and hemorrhagic shock and encephalopathy syndrome associated with an intronic deleti…
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A Clinical Study to Evaluate the Safety and Efficacy of ETX101 in Infants and Children With SCN1A-Po…
Drug Resistant Epilepsy: Clinical and Genetic Study
Natural History Study of Infants and Children With Developmental and Epileptic Encephalopathies
GABA Biomarkers in Dravet Syndrome
Expanded Access Use of Stiripentol in Dravet Syndrome or Sodium Channel Mutation Epileptic Encephalo…
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