The international primary ciliary dyskinesia (PCD) registry reports genotype/phenotype-correlations

Raidt J; Pennekamp P; Riepenhausen S; Krenz H; Helms S; Nöthe-Menchen T; Dworniczak B; Olbrich H; Loges NT; Große-Onnebrink J; Holgersen MG; Marthin JK; Nielsen KG; Dugas M; Omran H

Research article in edited proceedings (conference) | Peer reviewed

Details about the publication

PublisherEuropean Respiratory Journal
Book titleMonitoring airway disease (Volume 58)
Page rangePA2233-PA2233
Publishing companyEuropean Respiratory Society
Place of publicationonline
Editionsuppl 65
StatusPublished
Release year2021
Language in which the publication is writtenEnglish
ConferenceERS International Congress 2021, Virtuell, Online
DOI10.1183/13993003.congress-2021.PA2233
KeywordsGenetics; Bronchiectasis; Orphan diseases

Authors from the University of Münster

Dugas, Martin
Institute of Medical Informatics
Pennekamp, Petra
University Children's Hospital - Department for General Paediatrics
Riepenhausen, Sarah
Institute of Medical Informatics