Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
| Autor: | Bengtsson NE, Hall JK, Odom GL, Phelps MP, Andrus CR, Hawkins RD, Hauschka SD, Chamberlain JR, Chamberlain JS |
|---|---|
| Jazyk: | angličtina |
| Zdroj: | Nature communications [Nat Commun] 2017 Jun 23; Vol. 8, pp. 16007. Date of Electronic Publication: 2017 Jun 23. |
| DOI: | 10.1038/ncomms16007 |
| Abstrakt: | This corrects the article DOI: 10.1038/ncomms14454. |
| Databáze: | MEDLINE |
| Externí odkaz: |
|