Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation

Overview of attention for article published in Science Translational Medicine, July 2024

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SCGE researchers were part of a team that developed a genome editing therapy for progressive hearing loss caused by a human microRNA mutation. The AAV therapy improved hearing long term in mutant mice. #PublicationFriday https://t.co/IGcVgD1B9F https:/…

CRISPR gene editing technology has been successfully used to cure deafness in mice. https://t.co/5VWkHvGxD9

Breakthrough in hearing restoration! 🔬#Researchers have used CRISPR-Cas9 to correct mutations in the microRNA MIR96, linked to autosomal dominant deafness 50 (DFNA50), creating a potential #treatment for this form of inherited #hearingloss. More: https:/…

Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation | Science Translational Medicine https://t.co/0wFwzSv5OE

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