Researchers overcome hurdle in CRISPR gene editing for muscular dystrophy
Tuesday, January 8, 2019 - 19:30
in Health & Medicine
The gene editing technique known as CRISPR is a revolutionary approach to treating inherited diseases. However, the tool has yet to be used to effectively treat long-term, chronic conditions. A research team has identified and overcome a barrier in CRISPR gene editing that may lay the foundation for sustained treatments using the technique.