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All Day
Breakthroughs in Muscular Dystrophy
Join ASGCT and the Muscular Dystrophy Association in downtown Chicago for an unparalleled opportunity to delve into the latest advancements in research on gene and cell therapies for muscular dystrophy.
FDA Scientific Exchange 2024: Advancing Gene Editing Platforms for Rare Diseases
This Scientific Exchange with the FDA seeks to make progress on therapeutic development for rare conditions that are scientifically feasible but commercially non-viable.