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Learn MoreScn1b null mice are a model of a severe developmental and epileptic encephalopathy called Dravet Syndrome (DS). The goal of this study was to identify changes in gene expression between Scn1b wild-type and Scn1b null mice before seizure onset (postnatal day 10) SOURCE: Amanda Huber (hubera@umich.edu) - Benjamin Levi Lab University of Michigan
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