The Role of Specialized Pro-Resolving Mediators in Cystic Fibrosis Airways Disease
Cystic Fibrosis (CF) is a recessive genetic disease due to mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene encoding the CFTR chloride channel. The ion transport abnormalities related to CFTR mutation generate a dehydrated airway surface liquid (ASL) layer, which is r...
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| Main Authors: | , , |
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| Format: | Book |
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Frontiers Media S.A.,
2020-09-01T00:00:00Z.
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