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Dravet syndrome (severe myoclonic epilepsy of infancy), Scn1b mutated, in mouse (C57BL/6)

Cat.No.: AB50372
Species: Mus musculus (mouse)
Animal Type: mouse
Strain: C57BL/6
Target/Condition/Toxicity: Condition
Model Use: Dravet syndrome (severe myoclonic epilepsy of infancy)
Characteristic(Details): Mutated
Disease Area: Dravet syndrome (severe myoclonic epilepsy of infancy)
For research use only. Not intended for any clinical use.