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Treatment of Pulmonary Disease of Cystic Fibrosis: A Comprehensive Review
Cystic fibrosis (CF) is a genetic disease that causes absence or dysfunction of a protein named transmembrane conductance regulatory protein (CFTR) that works as an anion channel. As a result, the secretions of the organs where CFTR is expressed are very viscous, so their functionality is altered. T...
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| Publicat a: | Antibiotics (Basel) |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8144952/ https://ncbi.nlm.nih.gov/pubmed/33922413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/antibiotics10050486 |
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