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Dysregulated signalling pathways in innate immune cells with cystic fibrosis mutations
Cystic fibrosis (CF) is one of the most common life-limiting recessive genetic disorders in Caucasians, caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR). CF is a multi-organ disease that involves the lungs, pancreas, sweat glands, digestive and reproductive syste...
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| Publicat a: | Cell Mol Life Sci |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer International Publishing
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7599191/ https://ncbi.nlm.nih.gov/pubmed/32367193 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-020-03540-9 |
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