Unraveling the CFTR Function–Phenotype Connection for Precision Treatment in Cystic Fibrosis
Author:
Affiliation:
1. Department of PediatricsUniversity of Colorado Anschutz Medical CampusAurora, Coloradoand
2. Department of Internal MedicineUniversity of Kansas School of MedicineKansas City, Kansas
Publisher
American Thoracic Society
Subject
Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine
Link
https://www.atsjournals.org/doi/pdf/10.1164/rccm.201903-0696ED
Reference14 articles.
1. Origins of Cystic Fibrosis Lung Disease
2. New and emerging targeted therapies for cystic fibrosis
3. Sweat chloride as a biomarker of CFTR activity: Proof of concept and ivacaftor clinical trial data
4. Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype
5. Cystic Fibrosis Transmembrane Regulator Correctors and Potentiators
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