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Paper Details

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
PLoS Genet
182
2009
Dravet syndrome, FS, FS) gene, N641Y, Na(v)1, Na(v)1.7, SCN1A, SCN1A gene, SCN9A, Scn9a, Scn9a(, amino acid, amino acids, children, chromosome 2q24, clonic and tonic-clonic seizures, epilepsies, febrile seizure, febrile seizure (, febrile seizures, human, mice, missense variants, murine, murine Scn9a ortholog, p.N641Y, patients, seizure, severe myoclonic epilepsy of infancy

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Release 1.2