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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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| Publicado no: | Pediatr Pulmonol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | 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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