Science
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CRISPR Gene Editing Achieves Milestone: Scientists Successfully Reverse Hereditary Blindness in Clinical Trial
In a groundbreaking development that could transform the treatment of genetic diseases, researchers at the University of Cambridge have successfully used CRISPR-Cas9 gene editing to restore vision in patients with inherited retinal dystrophy, marking the first confirmed therapeutic use of gene editing in human eyes.
DW
Dr. David Whitfield