1. Liu, Jiali, Hayden, Melvin R, Yang, Ying. 2024. Research progress of RP1L1 gene in disease. In Gene, 912, 148367. doi:10.1016/j.gene.2024.148367. https://pubmed.ncbi.nlm.nih.gov/38485037/
2. Daniute, Ginte, Vilkeviciute, Alvita, Gedvilaite, Greta, Kriauciuniene, Loresa, Liutkeviciene, Rasa. 2021. RP1L1 rs3924612 gene polymorphism and RP1L1 protein associations among patients with early age-related macular degeneration. In Ophthalmic genetics, 43, 164-171. doi:10.1080/13816810.2021.2010770. https://pubmed.ncbi.nlm.nih.gov/34865606/
3. Koyanagi, Yoshito, Akiyama, Masato, Nishiguchi, Koji M, Kubo, Michiaki, Sonoda, Koh-Hei. 2019. Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients. In Journal of medical genetics, 56, 662-670. doi:10.1136/jmedgenet-2018-105691. https://pubmed.ncbi.nlm.nih.gov/31213501/
4. Li, Wei, He, Xiang-Dong, Yang, Zheng-Tao, Li, Jian-Kang, He, Wei. . De Novo Mutations Contributes Approximately 7% of Pathogenicity in Inherited Eye Diseases. In Investigative ophthalmology & visual science, 64, 5. doi:10.1167/iovs.64.2.5. https://pubmed.ncbi.nlm.nih.gov/36729443/
5. Hiraoka, Miki, Ishikawa, Aki, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Sakurai, Akihiro. 2020. A variant in the RP1L1 gene in a family with occult macular dystrophy in a predicted intrinsically disordered region. In Ophthalmic genetics, 41, 599-605. doi:10.1080/13816810.2020.1821383. https://pubmed.ncbi.nlm.nih.gov/32940107/
6. Miyake, Yozo, Tsunoda, Kazushige. 2015. Occult macular dystrophy. In Japanese journal of ophthalmology, 59, 71-80. doi:10.1007/s10384-015-0371-7. https://pubmed.ncbi.nlm.nih.gov/25665791/
7. Bowne, Sara J, Daiger, Stephen P, Malone, Kimberly A, Donovan, Danyel D, Sullivan, Lori S. 2003. Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene. In Molecular vision, 9, 129-37. doi:. https://pubmed.ncbi.nlm.nih.gov/12724644/
智鼠故事 
