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CFTR, Mucins, and Mucus Obstruction in Cystic Fibrosis
Mucus pathology in cystic fibrosis (CF) has been known for as long as the disease has been recognized and is sometimes called mucoviscidosis. The disease is marked by mucus hyperproduction and plugging in many organs, which are usually most fatal in the airways of CF patients, once the problem of me...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Cold Spring Harbor Laboratory Press
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3426818/ https://ncbi.nlm.nih.gov/pubmed/22951447 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a009589 |
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