DMD: Single CRISPR treatment provides long-term benefits in mice

Monday, February 18, 2019 - 15:12 in Health & Medicine

Researchers have shown that a single systemic treatment using CRISPR genome editing technology can safely and stably correct a genetic disease -- Duchenne muscular dystrophy (DMD) -- for more than a year in mice, despite observed immune responses and alternative gene editing outcomes.

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