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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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Bibliografiske detaljer
Udgivet i:Pediatr Pulmonol
Main Authors: Morrison, Cameron B., Markovetz, Matthew R., Ehre, Camille
Format: Artigo
Sprog:Inglês
Udgivet: 2019
Fag:
Online adgang: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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