Innovative Non-Viral Gene Editing: Harnessing Synthetic AAV Constructs
Time: 9:30 am
day: Day One 11th
Details:
- Explore how synthetic AAV genomes offer a novel approach to gene editing, providing a versatile platform for precise genetic modifications
- Discuss the potential of synthetic AAV constructs as efficient non-viral gene delivery vehicles, circumventing limitations associated with traditional viral vectors
- Uncover preclinical data for a non-CRISPR alternative to gene editing, paving the way for innovative treatments with enhanced safety and efficacy profiles