CRISPR Edits Genes in Fetal Monkeys, Advances Cure for Genetic Diseases

Apr 23, 2024, 01:51 PM

Recent advancements in CRISPR technology have brought the possibility of curing genetic diseases before birth closer to reality, with successful experiments conducted on fetal monkeys. Researchers achieved a scientific milestone by using CRISPR base editing to treat liver disease in these subjects. This breakthrough in genome editing has been recognized as a crucial step towards addressing genetic diseases as a significant public health challenge.