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Applications of CRISPR/Cas9 in retinal degenerative diseases
Gene therapy is a potentially effective treatment for retinal degenerative diseases. Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system has been developed as a new genome-editing tool in ophthalmic studies. Recent advances in researches showe...
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| Veröffentlicht in: | Int J Ophthalmol |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
International Journal of Ophthalmology Press
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5406646/ https://ncbi.nlm.nih.gov/pubmed/28503441 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2017.04.23 |
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