Abstract
cystic fibrosis (CF) is caused by severe loss-of-function mutations in the CFTR chloride channel ([9][1]). The predominant life-limiting pathology in CF patients is recurrent bacterial infections in the airways, which is attributable at least in part to reduced mucociliary clearance by the
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have