Defective epithelial ion transport is the hallmark of the common life-limiting genetic disease cystic fibrosis (CF). CF is caused by dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR), an ATP-binding cassette transporter, which functions as...
CITATION STYLE
Al Salmani, M. K., Sondo, E., Balut, C., Sheppard, D. N., Singh, A. K., & Pedemonte, N. (2020). Molecular Physiology and Pharmacology of the Cystic Fibrosis Transmembrane Conductance Regulator (pp. 605–670). https://doi.org/10.1007/978-3-030-55454-5_16
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