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1. Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children

3. The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthrough

5. RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiology

9. miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR‐101 that regulate WISP1 expression.

10. Large phenotypic spectrum associated with two new deep intronic variants on the CFTR gene

11. Additional file 3: Table S2. of DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

12. Additional file 2: Figure S2. of DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

15. DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

19. The RNA Binding Protein Tristetraprolin Contributes to CFTR mRNA Stability in Cystic Fibrosis.

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