Researchers overcome hurdle in CRISPR gene editing for muscular dystrophy

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.

Source: sciencedaily.com

Related posts

Physicists propose path to faster, more flexible robots

Better medical record-keeping needed to fight antibiotic overuse

Global life expectancy to increase by nearly 5 years by 2050 despite geopolitical, metabolic, and environmental threats