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. 2016 May 23;8:59. doi: 10.1186/s13073-016-0316-x

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© Maggio et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Milestones on the path towards somatic genetic therapies for Duchenne muscular dystrophy that rely on viral-based DMD editing. The time marks correspond to the first release date of the referenced articles (for example, advanced online publication). AdV adenoviral vector, CRISPR–Cas9 clustered regularly interspaced short palindromic repeat-associated Cas9 nuclease, DMD Duchenne muscular dystrophy, DSB double-stranded DNA break, HE homing endonuclease, rAAV recombinant adeno-associated virus, TALE transcription activator-like effector