A groundbreaking gene-editing method from UT Austin is changing the game for treating complex genetic diseases like cystic fibrosis, hemophilia, and Tay Sachs. Using retrons—DNA tools borrowed from bacteria—scientists can now replace entire damaged sections of DNA in a single step. This means faster, more inclusive therapies that can help thousands of patients with rare or hard-to-target mutations. With editing efficiency jumping from 1.5% to 30%, this could be the future of gene therapy!<br />WooGlobe Ref : WGA660933<br />For licensing and to use this video, please email licensing@wooglobe.com
