Neuromuscular disease: Genome editing shows promise in an in vivo model of Duchenne muscular dystrophy
- PMID: 26782331
- DOI: 10.1038/nrneurol.2016.4
Neuromuscular disease: Genome editing shows promise in an in vivo model of Duchenne muscular dystrophy
Comment on
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Multiplex CRISPR/Cas9-based genome editing for correction of dystrophin mutations that cause Duchenne muscular dystrophy.Nat Commun. 2015 Feb 18;6:6244. doi: 10.1038/ncomms7244. Nat Commun. 2015. PMID: 25692716 Free PMC article.
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