Researchers overcome hurdle in CRISPR gene editing for muscular dystrophy

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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.

from Latest Science News -- ScienceDaily http://bit.ly/2FgknpY

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