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The CFTR and ENaC debate: how important is ENaC in CF lung disease?
Cystic fibrosis (CF) is caused by the loss of the cystic fibrosis transmembrane conductance regulator (CFTR) function and results in a respiratory phenotype that is characterized by dehydrated mucus and bacterial infections that affect CF patients throughout their lives. Much of the morbidity and mo...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Physiological Society
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3379041/ https://ncbi.nlm.nih.gov/pubmed/22492740 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00036.2012 |
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