Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping.
Saved in:
| Title: | Preclinical development of genome editing to treat Duchenne muscular dystrophy by exon skipping. |
|---|---|
| Authors: | Padmaswari MH; Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.; Cell and Molecular Biology, University of Arkansas, Fayetteville, AR, USA., Agrawal S; Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA., Nelson CE; Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.; Cell and Molecular Biology, University of Arkansas, Fayetteville, AR, USA. |
| Source: | Journal of neuromuscular diseases [J Neuromuscul Dis] 2025 May; Vol. 12 (3), pp. 424-434. Date of Electronic Publication: 2025 Mar 19. |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: IOS Press Country of Publication: United States NLM ID: 101649948 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2214-3602 (Electronic) Linking ISSN: 22143599 NLM ISO Abbreviation: J Neuromuscul Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 2214-3602 |
|---|---|
| DOI: | 10.1177/22143602251326993 |
