Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties via hydration. Morrison CB, Shaffer KM, Araba KC, Markovetz MR, et al. Eur Respir J 2022;59.

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Amedeo Smart

Independent Medical Education

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Morrison CB, Shaffer KM, Araba KC, Markovetz MR, et al. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties via hydration. Eur Respir J 2022;59.
PMID: 34172469