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Keywords: mucus transport, mucus viscosity, cystic fibrosis, bicarbonate, glutathione Cystic fibrosis (CF) is an autosomal recessive disease caused by absent or dysfunctional CFTR (cystic fibrosis transmembrane conductance regulator) protein, an ion channel that regulates the secretion of chloride, bicarbonate (1), and other molecules such as glutathione (2) across the epithelial cell surface
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