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Managing Fungal Infections in Cystic Fibrosis Patients: Challenges in Clinical Practice
Cystic Fibrosis (CF) is an autosomal recessive disease characterized by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Impairment of the CFTR protein in the respiratory tract results in the formation of thick mucus, development of inflammation, destruction of b...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Dove
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998013/ https://www.ncbi.nlm.nih.gov/pubmed/33790585 http://dx.doi.org/10.2147/IDR.S267219 |