Format

Send to

Choose Destination
Eur Respir J. 2017 Dec 28;50(6). pii: 1700426. doi: 10.1183/13993003.00426-2017. Print 2017 Dec.

An informative intragenic microsatellite marker suggests the IL-1 receptor as a genetic modifier in cystic fibrosis.

Author information

1
Dept of Pediatric Pneumology, Neonatology and Allergology, Hannover Medical School, Hannover, Germany mekus.frauke@mh-hannover.de.
2
Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), German Centre for Lung Research, Hannover, Germany.
3
Pediatric Infectiology, Immunology, and Cystic Fibrosis, Children's Hospital of the University of Tübingen, Tübingen, Germany.
4
Dept of Pediatric Pneumology, Neonatology and Allergology, Hannover Medical School, Hannover, Germany.
5
Dept of Pediatric Pneumology, Hauner Children's Hospital, University of Munich, Munich, Germany.
6
Comprehensive Pneumology Center (CPC), German Center for Lung Research (DZL), Munich, Germany.
7
Dept of Translational Pulmonology, Translational Lung Research Center Heidelberg (TLRC), German Center for Lung Research (DZL), University of Heidelberg, Heidelberg, Germany.
8
Division of Pediatric Pulmonology and Allergy and Cystic Fibrosis Center, Dept of Pediatrics, University of Heidelberg, Heidelberg, Germany.
9
Dept of Pediatric Pulmonology and Immunology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Conflict of interest statement

Conflict of interest: Disclosures can be found alongside this article at erj.ersjournals.com

Supplemental Content

Full text links

Icon for HighWire
Loading ...
Support Center