Developmental and epileptic encephalopathies (DEEs) are a group of epileptic disorders characterized by the co-occurrence of seizures and intellectual disability. We aim to determine the pathogenic mechanism by which a novel, recurrent missense variant in CUX2, a transcription factor (TF), causes DEEs using a patient induced pluripotent stem cell-derived neuronal model. The insights gained from this project will expand our knowledge on TFs in epilepsy, potentially inspiring new strategies for the development of therapeutics.
|Effective start/end date||7/1/20 → 6/30/21|
- American Epilepsy Society (Agmt 5/13/20)
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