Home•Our Research•Publications•Life-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene

Life-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene

Thematic Area:
Therapeutics
Disease Area:
Rare Neurological Disorders
Research Focus:
Drug Discovery
Collaborators:
Academic