Metabolomic responses to lumacaftor/ivacaftor in cystic fibrosis

Kopp, BT; McCulloch, S; Shrestha, CL; Zhang, SZ; Sarzynski, L; Woodley, FW; Hayes, D

Kopp, BT (reprint author), Nationwide Childrens Hosp, W510,700 Childrens Dr, Columbus, OH 43205 USA.

PEDIATRIC PULMONOLOGY, 2018; 53 (5): 583

Abstract

BackgroundCystic fibrosis (CF) is a life-limiting disease caused by a defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. L......

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