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A frequent ancestral intronic founder variant in DNAI1 causes primary ciliary dyskinesia

Year: 2026

Type: article

Source: European Respiratory Journal

DOI: 10.1183/13993003.01575-2026

Authors: Niki T. Loges, Ina Baumann, Dörthe Thüß, Gerard W. Dougherty, Kim G. Nielsen, June K. Marthin, Nikhita Damaraju, Johanna Raidt, Heike Olbrich, Petra Pennekamp, Bernd Dworniczak, Maren Spaeter, Dominik Otto, Barbara L. Zimmer, Monika H. Tedy, Retno D. Tenardi-Wenge, Danny E. Miller, Heymut Omran

Institutions: University Hospital Münster, University of Copenhagen, Copenhagen University Hospital, Rigshospitalet, Seattle Children's Hospital, University of Washington, Brotman Baty Institute

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, NIH Clinical Center

OpenAlex ID: W7224538462

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