1. Zhu, Dongliang, Zhang, Hongguo, Wang, Ruixue, Liu, Ruizhi, Zhang, Guirong. 2019. Association of DNAH11 gene polymorphisms with asthenozoospermia in Northeast Chinese patients. In Bioscience reports, 39, . doi:10.1042/BSR20181450. https://pubmed.ncbi.nlm.nih.gov/31160482/
2. Lai, Michele, Pifferi, Massimo, Bush, Andrew, Boner, Attilio, Pistello, Mauro. 2016. Gene editing of DNAH11 restores normal cilia motility in primary ciliary dyskinesia. In Journal of medical genetics, 53, 242-9. doi:10.1136/jmedgenet-2015-103539. https://pubmed.ncbi.nlm.nih.gov/26729821/
3. Guan, Yuhong, Yang, Haiming, Yao, Xingfeng, Ge, Wentong, Ni, Xin. 2021. Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in China. In Chest, 159, 1768-1781. doi:10.1016/j.chest.2021.02.006. https://pubmed.ncbi.nlm.nih.gov/33577779/
4. Dong, Shumei, Bei, Fei, Yu, Tingting, Chen, Xiafang, Yan, Hui. 2022. A Novel Compound Heterozygous Mutation in the DNAH11 Gene Found in Neonatal Twins With Primary Ciliary Dyskinesis. In Frontiers in genetics, 13, 814511. doi:10.3389/fgene.2022.814511. https://pubmed.ncbi.nlm.nih.gov/35295944/
5. Guo, Senzhao, Tang, Dongdong, Chen, Yuge, Sha, Yanwei, Lv, Mingrong. 2024. Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility. In Human genomics, 18, 97. doi:10.1186/s40246-024-00658-w. https://pubmed.ncbi.nlm.nih.gov/39256880/
6. Schultz, Rüdiger, Elenius, Varpu, Lukkarinen, Heikki, Saarela, Tanja. 2020. Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype. In BMC medical genetics, 21, 237. doi:10.1186/s12881-020-01171-2. https://pubmed.ncbi.nlm.nih.gov/33243178/
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