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Start codon disruption with CRISPR/Cas9 prevents murine Fuchs’ endothelial corneal dystrophy
A missense mutation of collagen type VIII alpha 2 chain (COL8A2) gene leads to early-onset Fuchs’ endothelial corneal dystrophy (FECD), which progressively impairs vision through the loss of corneal endothelial cells. We demonstrate that CRISPR/Cas9-based postnatal gene editing achieves structural a...
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| Publicat a: | eLife |
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| Autors principals: | , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
eLife Sciences Publications, Ltd
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8216720/ https://ncbi.nlm.nih.gov/pubmed/34100716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.55637 |
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