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. 2017 Jun 23;8:16007. doi: 10.1038/ncomms16007

Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy

Niclas E Bengtsson, John K Hall, Guy L Odom, Michael P Phelps, Colin R Andrus, R David Hawkins, Stephen D Hauschka, Joel R Chamberlain, Jeffrey S Chamberlain
PMCID: PMC5489999  PMID: 28643790

Nature Communications 8: Article number: 14454; DOI: 10.1038/ncomms14454 (2017); Published: February 14 2017; Updated: June 23 2017

This Article contains an error in Fig. 4, for which we apologize. In panel a, the image reporting dystrophin labelling following SaCas9Δ5253 treatment was inadvertently duplicated from the corresponding image following SpCas9/Δ5253 treatment. The correct version of this figure appears below as Fig. 1. The raw data associated with this experiment are provided as a separate Supplementary Data file.

Figure 1.

Figure 1

Supplementary Material

Supplementary Data 1
ncomms16007-s1.pdf (7.2MB, pdf)

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Data 1
ncomms16007-s1.pdf (7.2MB, pdf)

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