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SCN1A
Dravet
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Dravet Syndrome
Symptoms
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Epilepsy
SCN9A
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Disease
Channelopathy
Channelopathies
Rare Genetic
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CDKL5
Mutation
Recessive
Mutation
DNA Mutations
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SCN1A
Protein
Nocturnal Frontal
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Epilepsy
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Mutations
KCNQ2
Mutation
SCN4A
Gene
Genetic Eye
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Normal Brain
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