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Explore the cutting-edge genome editing techniques of CRISPR/Cas9 gene therapy and CAR T-cell therapy (CART) in this informative 13-minute video. Delve into the promising research and therapeutic applications for sickle cell disease and other genetic disorders. Learn about the recent FDA approval of Exa-cel, a gene-editing technique for sickle cell anemia. Gain insights into these revolutionary lab techniques that are shaping the future of genetic medicine and offering new hope for patients with previously untreatable conditions.
