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Mechanistic, phenotypic and therapeutic insights in SCN2A-related epilepsy, autism, and developmental delay.

Stephan J. Sanders, BBMS, PhD 
Assistant Professor of Psychiatry,
University of California, San Francisco

and

Kevin Bender, PhD
Associate Professor of Neurology
University of California, San Francisco

Learning objectives

By the end of the session, participants will be able to:

  • Describe the contribution of SCN2A mutations to cases of epilepsy, autism, and developmental delay 
  • Describe the relationship between the functional impacts of SCN2A mutations and clinical symptoms 
  • Describe the impact of loss-of-function variants on neurobiology

Event Details

  • Bridgetta Catania

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