1. Pennarun, G, Chapelin, C, Escudier, E, Amselem, S, Duriez, B. . The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia. In Human genetics, 107, 642-9. doi:. https://pubmed.ncbi.nlm.nih.gov/11153919/
2. Rocca, Maria Santa, Piatti, Gioia, Michelucci, Angela, Valetto, Angelo, Foresta, Carlo. 2020. A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report. In BMC medical genetics, 21, 220. doi:10.1186/s12881-020-01160-5. https://pubmed.ncbi.nlm.nih.gov/33167880/
3. Lv, Yanhua, Liu, Yanqing, Wang, Yueqiang, Pang, Qiuxiang, Hu, Guirong. 2021. CCDC114, DNAI2 and TOP2A involves in the effects of tibolone treatment on postmenopausal endometrium. In BMC women's health, 21, 240. doi:10.1186/s12905-020-01156-6. https://pubmed.ncbi.nlm.nih.gov/34116668/
4. Che Ismail, C L, Yusof, N Y, Mat Lazim, N, Alwi, Z B, Abdullah, B. . Exploring nasopharyngeal carcinoma genetics: Bioinformatics insights into pathways and gene associations. In The Medical journal of Malaysia, 79, 615-625. doi:. https://pubmed.ncbi.nlm.nih.gov/39352166/
5. Al-Mutairi, Dalal A, Alsabah, Basel H, Alkhaledi, Bashar A, Pennekamp, Petra, Omran, Heymut. 2022. Identification of a novel founder variant in DNAI2 cause primary ciliary dyskinesia in five consanguineous families derived from a single tribe descendant of Arabian Peninsula. In Frontiers in genetics, 13, 1017280. doi:10.3389/fgene.2022.1017280. https://pubmed.ncbi.nlm.nih.gov/36303540/
6. Loges, Niki Tomas, Olbrich, Heike, Fenske, Lale, Mitchison, Hannah M, Omran, Heymut. 2008. DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm. In American journal of human genetics, 83, 547-58. doi:10.1016/j.ajhg.2008.10.001. https://pubmed.ncbi.nlm.nih.gov/18950741/