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The Distribution and Role of the CFTR Protein in the Intracellular Compartments
Cystic fibrosis is a hereditary disease that mainly affects secretory organs in humans. It is caused by mutations in the gene encoding CFTR with the most common phenylalanine deletion at position 508. CFTR is an anion channel mainly conducting Cl(−) across the apical membranes of many different epit...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618639/ https://www.ncbi.nlm.nih.gov/pubmed/34832033 http://dx.doi.org/10.3390/membranes11110804 |