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

Nature Communications 8: Article number: 14454 (2017); Published: 14 February 2017; Updated: 23 June 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 corre...

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Autores principales:	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
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2017
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/77235027c66448b889ec5dc2c4163e56
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spelling	oai:doaj.org-article:77235027c66448b889ec5dc2c4163e562021-12-02T15:38:50ZCorrection: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy10.1038/ncomms160072041-1723https://doaj.org/article/77235027c66448b889ec5dc2c4163e562017-06-01T00:00:00Zhttps://doi.org/10.1038/ncomms16007https://doaj.org/toc/2041-1723Nature Communications 8: Article number: 14454 (2017); Published: 14 February 2017; Updated: 23 June 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.Niclas E. BengtssonJohn K. HallGuy L. OdomMichael P. PhelpsColin R. AndrusR. David HawkinsStephen D. HauschkaJoel R. ChamberlainJeffrey S. ChamberlainNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-1 (2017)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q 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 Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
description	Nature Communications 8: Article number: 14454 (2017); Published: 14 February 2017; Updated: 23 June 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.
format	article
author	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
author_facet	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
author_sort	Niclas E. Bengtsson
title	Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
title_short	Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
title_full	Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
title_fullStr	Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
title_full_unstemmed	Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
title_sort	correction: corrigendum: muscle-specific crispr/cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for duchenne muscular dystrophy
publisher	Nature Portfolio
publishDate	2017
url	https://doaj.org/article/77235027c66448b889ec5dc2c4163e56
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Correction: Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy

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