1. Raidt, Johanna, Riepenhausen, Sarah, Pennekamp, Petra, Nielsen, Kim G, Omran, Heymut. 2024. Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations. In The European respiratory journal, 64, . doi:10.1183/13993003.01769-2023. https://pubmed.ncbi.nlm.nih.gov/38871375/
2. Zhou, Nannan, Liang, Weilin, Zhang, Yanzhu, Cui, Haiyan, Cheng, Yuanxiong. 2023. ODAD1 variants resulting from splice-site mutations retain partial function and cause primary ciliary dyskinesia with outer dynein arm defects. In Frontiers in genetics, 14, 1270278. doi:10.3389/fgene.2023.1270278. https://pubmed.ncbi.nlm.nih.gov/38028630/
3. Ostrowski, Lawrence E, Yin, Weining, Smith, Amanda J, Zariwala, Maimoona A, Knowles, Michael R. 2022. Expression of a Truncated Form of ODAD1 Associated with an Unusually Mild Primary Ciliary Dyskinesia Phenotype. In International journal of molecular sciences, 23, . doi:10.3390/ijms23031753. https://pubmed.ncbi.nlm.nih.gov/35163670/
4. Navapour, Leila, Mogharrab, Navid, Parvin, Ali, Taheri-Anganeh, Mortaza, Ghasemnejad-Berenji, Hojat. 2024. Identification of high-risk non-synonymous SNPs (nsSNPs) in DNAH1 and DNAH17 genes associated with male infertility: a bioinformatics analysis. In Journal of applied genetics, , . doi:10.1007/s13353-024-00884-x. https://pubmed.ncbi.nlm.nih.gov/38874855/
5. Onoufriadis, Alexandros, Paff, Tamara, Antony, Dinu, Pals, Gerard, Mitchison, Hannah M. 2012. Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia. In American journal of human genetics, 92, 88-98. doi:10.1016/j.ajhg.2012.11.002. https://pubmed.ncbi.nlm.nih.gov/23261303/
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