NACFC 2022 | W36: Genetic and Cell-Based Approaches to Cystic Fibrosis Therapy
In this workshop, we will explore how genetic therapies are being used to repair or augment mutated CFTR. We also explore emerging cell-based therapeutic approaches with applications for ex vivo gene editing and engraftment. Originally recorded November 5, 2022.
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NACFC 2022 | W21: Evidence-Based Medicine: Update on Clinical Trials in Cystic Fibrosis
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NACFC 2022 | S09: Being on the Spectrum: CFTR-Related Disorders Revisited
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VLC 2026 | Treating Cystic Fibrosis at the Source: Today’s Therapies and Tomorrow’s Technologies
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NACFC 2024 | DG08: Updates & Resources for Genetic Counseling for CF, CRMS/CFSPID
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