Pathological mucus and impaired mucus clearance in cystic fibrosis patients result from increased concentration, not altered pH
Cystic fibrosis (CF) is a recessive genetic disease that is characterised by airway mucus plugging and reduced mucus clearance. There are currently alternative hypotheses that attempt to describe the abnormally viscous and elastic mucus that is a hallmark of CF airways disease, including: 1) loss of...
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Veröffentlicht in: | The European respiratory journal 2018-12, Vol.52 (6), p.1801297 |
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