1. Ohno, Tomoko, Meguro, Akira, Takeuchi, Masaki, Okinami, Satoshi, Mizuki, Nobuhisa. 2018. Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients. In Ocular immunology and inflammation, 27, 699-705. doi:10.1080/09273948.2018.1523438. https://pubmed.ncbi.nlm.nih.gov/30395750/
2. Latour, Brooke L, Van De Weghe, Julie C, Rusterholz, Tamara Ds, Roepman, Ronald, Doherty, Dan. . Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome. In The Journal of clinical investigation, 130, 4423-4439. doi:10.1172/JCI131656. https://pubmed.ncbi.nlm.nih.gov/32453716/
3. Wang, Hao, Luo, Guanjun, Hu, Wensheng, Zhao, Yong, Qi, Ming. 2022. Whole Exome Sequencing Identified Novel ARMC9 Variations in Two Cases With Joubert Syndrome. In Frontiers in genetics, 13, 817153. doi:10.3389/fgene.2022.817153. https://pubmed.ncbi.nlm.nih.gov/35186037/
4. Kar, Anjana, Phadke, Shubha R, Das Bhowmik, Aneek, Dalal, Ashwin. 2017. Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly. In American journal of medical genetics. Part A, 176, 34-40. doi:10.1002/ajmg.a.38537. https://pubmed.ncbi.nlm.nih.gov/29159890/
5. Aksu Uzunhan, Tuğçe, Ertürk, Biray, Aydın, Kürşad, Yüksel, Atıl, Kayserili, Hülya. 2022. Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome. In Clinical neurology and neurosurgery, 224, 107560. doi:10.1016/j.clineuro.2022.107560. https://pubmed.ncbi.nlm.nih.gov/36580738/
6. Zhao, Dengzhi, Chu, Yan, Yang, Ke, Xiao, Hai, Liao, Shixiu. . [Clinical features and genetic analysis of two Chinese pedigrees affected with Joubert syndrome]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 40, 21-25. doi:10.3760/cma.j.cn511374-20220122-00055. https://pubmed.ncbi.nlm.nih.gov/36584995/
7. Skuladottir, Astros Th, Bjornsdottir, Gyda, Nawaz, Muhammad Sulaman, Stefansson, Hreinn, Stefansson, Kari. 2021. A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo. In Communications biology, 4, 1148. doi:10.1038/s42003-021-02673-2. https://pubmed.ncbi.nlm.nih.gov/34620984/
8. Elghzaly, Ashraf A, Sun, Celi, Looger, Loren L, Ragab, Gaafar, Nath, Swapan K. 2022. Genome-wide association study for systemic lupus erythematosus in an egyptian population. In Frontiers in genetics, 13, 948505. doi:10.3389/fgene.2022.948505. https://pubmed.ncbi.nlm.nih.gov/36324510/
智鼠故事 
