Phenotype-genotype associations in primary ciliary dyskinesia: where do we stand?

Eur Respir J. 2021 Aug 5;58(2):2100392. doi: 10.1183/13993003.00392-2021. Print 2021 Aug.

Authors

Myrofora Goutaki^{1

2}, Eva S L Pedersen¹

Affiliations

¹ Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
² Paediatric Respiratory Medicine, Children's University Hospital of Bern, University of Bern, Bern, Switzerland.

PMID: 34353866
DOI: 10.1183/13993003.00392-2021

No abstract available

Publication types

Editorial
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Ciliary Motility Disorders*
Genotype
Humans
Kartagener Syndrome* / diagnosis
Kartagener Syndrome* / genetics
Phenotype