Duchenne muscular dystrophy awaits gene therapy

Solid’s gene therapy disappoints in the clinic, but other gene therapies and exon-skipping agents continue their march, with CRISPR on the way.

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Correspondence to Dan Jones.

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Jones, D. Duchenne muscular dystrophy awaits gene therapy. Nat Biotechnol 37, 335–337 (2019). https://doi.org/10.1038/s41587-019-0103-5

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