Emerging pharmacotherapies in cystic fibrosis
Author:
Affiliation:
1. Irish Centre for Genetic Lung Disease, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland
Funder
Royal College of Surgeons in Ireland
Publisher
Informa UK Limited
Subject
Public Health, Environmental and Occupational Health,Pulmonary and Respiratory Medicine,Immunology and Allergy
Link
https://www.tandfonline.com/doi/pdf/10.1080/17476348.2018.1512409
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2. The relative frequency of CFTR mutation classes in European patients with cystic fibrosis
3. Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene
4. Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease
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