Learning Objectives:

  1. Understand how adeno-associated viruses (AAV) are used as gene therapy vectors.
  2. Have a basic understanding of the current state-of-the art potential of AAV vectors to treat neurological diseases
  3. Have a basic understanding of the current limitations of AAV vectors to treat neurological diseases
Session date: 
01/08/2025 - 8:00am to 9:00am CST
Location: 
UT Southwestern Medical Center
Dallas, TX
United States
See map: Google Maps
Add to calendar: 
  • 1.00 AMA
  • 1.00 Attendance
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