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Mucus, Mucins and Cystic Fibrosis

Cystic fibrosis (CF) is both the most common and most lethal genetic disease in the Caucasian population. CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and is characterized by the accumulation of thick, adherent mucus plaques in multiple organs, of...

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Bibliographic Details
Published in:Pediatr Pulmonol
Main Authors: Morrison, Cameron B., Markovetz, Matthew R., Ehre, Camille
Format: Artigo
Language:Inglês
Published: 2019
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6853602/
https://ncbi.nlm.nih.gov/pubmed/31715083
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ppul.24530
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