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ERJ Open Research|August 19, 2022
The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTNJohanna Raidt, Bernard Maitre, Petra Pennekamp, et al.
American Journal of Human Genetics|July 30, 2013
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6Maimoona A Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, et al.
The European Respiratory Journal|June 13, 2024
Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlationsJohanna Raidt, Sarah Riepenhausen, Petra Pennekamp, et al.
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