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Author

Vrishti Sinha

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Open access Aug 2026

Double-stranded DNA donors and CRISPR-Cas9 for universal correction of mutations causing cystic fibrosis in human airway cells

These results demonstrate that low levels of CFTR integration can be made therapeutically relevant by optimizing the designs of gene editing reagents, an essential step toward in vivo gene therapy for CF.

Vrishti Sinha, P. Ayoub, C. Juett et al. · 0 citations

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