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

Abstract:

:This corrects the article DOI: 10.1038/ncomms14454.

journal_name

Nat Commun

journal_title

Nature communications

authors

Bengtsson NE,Hall JK,Odom GL,Phelps MP,Andrus CR,Hawkins RD,Hauschka SD,Chamberlain JR,Chamberlain JS

doi

10.1038/ncomms16007

subject

Has Abstract

pub_date

2017-06-23 00:00:00

pages

16007

issn

2041-1723

pii

ncomms16007

journal_volume

8

pub_type

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