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Prime editing-mediated correction of the CFTR W1282X mutation in iPSCs and derived airway epithelial cells
A major unmet need in the cystic fibrosis (CF) therapeutic landscape is the lack of effective treatments for nonsense CFTR mutations, which affect approximately 10% of CF patients. Correction of nonsense CFTR mutations via genomic editing represents a promising therapeutic approach. In this study, w...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686454/ https://www.ncbi.nlm.nih.gov/pubmed/38019847 http://dx.doi.org/10.1371/journal.pone.0295009 |