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pro vyhledávání: '"E. F. McKone"'
Autor:
R. Reilly, M. S. Mroz, E. Dempsey, K. Wynne, S. J. Keely, E. F. McKone, C. Hiebel, C. Behl, J. A. Coppinger
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Abstract Deletion of phenylalanine 508 of the cystic fibrosis transmembrane conductance regulator (ΔF508 CFTR) is a major cause of cystic fibrosis (CF), one of the most common inherited childhood diseases. ΔF508 CFTR is a trafficking mutant that is
Externí odkaz:
https://doaj.org/article/83f7d91151ee4471ab8b716bf6da8bf0
Publikováno v:
Journal of Cystic Fibrosis. (2):147-153
Background Centralized spirometry may significantly improve quality of spirometry and reduce variability of this outcome measure in clinical trials in cystic fibrosis (CF). Methods Spirometry was performed during the phase 2 randomized, placebo-contr