Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis

Author:

McCague Allison F.1,Raraigh Karen S.1,Pellicore Matthew J.1,Davis-Marcisak Emily F.1,Evans Taylor A.1,Han Sangwoo T.1,Lu Zhongzhou1,Joynt Anya T.1,Sharma Neeraj1,Castellani Carlo2,Collaco Joseph M.3,Corey Mary4,Lewis Michelle H.5,Penland Chris M.6,Rommens Johanna M.7,Stephenson Anne L.8,Sosnay Patrick R.9,Cutting Garry R.1ORCID

Affiliation:

1. McKusick-Nathans Institute of Genetic Medicine, School of Medicine

2. Cystic Fibrosis Center, IRCCS Istituto Giannina Gaslini, Genoa, Italy

3. Eudowood Division of Pediatric Respiratory Sciences, School of Medicine

4. Research Institute and

5. Berman Institute of Bioethics, and

6. Cystic Fibrosis Foundation, Bethesda, Maryland; and

7. Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada

8. Department of Respirology, Adult Cystic Fibrosis Program, St. Michael’s Hospital, Toronto, Ontario, Canada

9. Pulmonary and Critical Care Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

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