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Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder

Cystic fibrosis patients exhibit lung disease consistent with a failure of innate airway defense mechanisms. The link between abnormal ion transport and disease initiation and progression is not fully understood, but airway mucus dehydration seems paramount in the initiation of CF lung disease. New...

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Main Authors: Clunes, Mark T., Boucher, Richard C.
格式: Artigo
語言:Inglês
出版: 2007
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2430075/
https://ncbi.nlm.nih.gov/pubmed/18560471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ddmec.2007.09.001
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