1. Gianesello, Lisa, Del Prete, Dorella, Ceol, Monica, Calò, Lorenzo Arcangelo, Anglani, Franca. 2020. From protein uptake to Dent disease: An overview of the CLCN5 gene. In Gene, 747, 144662. doi:10.1016/j.gene.2020.144662. https://pubmed.ncbi.nlm.nih.gov/32289351/
2. Mansour-Hendili, Lamisse, Blanchard, Anne, Le Pottier, Nelly, Jeunemaître, Xavier, Vargas-Poussou, Rosa. 2015. Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1. In Human mutation, 36, 743-52. doi:10.1002/humu.22804. https://pubmed.ncbi.nlm.nih.gov/25907713/
3. Mollataheri, Ali, Mojbafan, Marzieh, Hosseini, Rozita, Mousavi, Mohammad, Otoukesh, Hasan. 2023. A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations. In Nephron, 147, 470-477. doi:10.1159/000528344. https://pubmed.ncbi.nlm.nih.gov/36646056/
4. Inoue, Tomohiko, Nagano, China, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai. 2020. Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1. In Clinical and experimental nephrology, 24, 606-612. doi:10.1007/s10157-020-01876-x. https://pubmed.ncbi.nlm.nih.gov/32201916/
5. Zhai, Panpan, Lv, Weigang, Yang, Xiaoqing, Ding, Ying, Huang, Yanshi. 2022. Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene. In Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society, 25, 397-403. doi:10.1177/10935266211065554. https://pubmed.ncbi.nlm.nih.gov/35100899/
6. Marik, Binata, Bagga, Arvind, Sinha, Aditi, Hari, Pankaj, Sharma, Arundhati. 2022. Genetic and clinical profile of patients with hypophosphatemic rickets. In European journal of medical genetics, 65, 104540. doi:10.1016/j.ejmg.2022.104540. https://pubmed.ncbi.nlm.nih.gov/35738466/
7. Fischer, Anne Sophie, Marcussen, Niels, Rasmussen, Maria, Randers, Else. 2017. Two brothers with identical variants of the CLCN5 gene-one developing Dent's disease. In Clinical kidney journal, 11, 459-461. doi:10.1093/ckj/sfx123. https://pubmed.ncbi.nlm.nih.gov/30094009/
8. Fisher, S E, van Bakel, I, Lloyd, S E, Thakker, R V, Craig, I W. . Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). In Genomics, 29, 598-606. doi:. https://pubmed.ncbi.nlm.nih.gov/8575751/
9. Devuyst, Olivier, Thakker, Rajesh V. 2010. Dent's disease. In Orphanet journal of rare diseases, 5, 28. doi:10.1186/1750-1172-5-28. https://pubmed.ncbi.nlm.nih.gov/20946626/
10. Zhang, Hao, Wang, Chun, Yue, Hua, Zhang, Zeng, Zhang, Zhen-Lin. . Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent-1 disease. In Nephrology (Carlton, Vic.), 19, 80-3. doi:10.1111/nep.12179. https://pubmed.ncbi.nlm.nih.gov/24428215/