1. Wagner, Carsten A, Unwin, Robert, Lopez-Garcia, Sergio C, Bockenhauer, Detlef, Walsh, Stephen. 2023. The pathophysiology of distal renal tubular acidosis. In Nature reviews. Nephrology, 19, 384-400. doi:10.1038/s41581-023-00699-9. https://pubmed.ncbi.nlm.nih.gov/37016093/
2. Bourgeois, Soline, Bettoni, Carla, Baron, Stéphanie, Wagner, Carsten A. 2018. Haploinsufficiency of the Mouse Atp6v1b1 Gene Leads to a Mild Acid-Base Disturbance with Implications for Kidney Stone Disease. In Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 47, 1095-1107. doi:10.1159/000490186. https://pubmed.ncbi.nlm.nih.gov/29843146/
3. 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/
4. Cogal, Andrea G, Arroyo, Jennifer, Shah, Ronak Jagdeep, Lieske, John C, Harris, Peter C. 2021. Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease. In Kidney international reports, 6, 2862-2884. doi:10.1016/j.ekir.2021.08.033. https://pubmed.ncbi.nlm.nih.gov/34805638/
5. Elia, Avraam, Voskarides, Konstantinos, Demosthenous, Panayiota, Pierides, Alkis, Deltas, Constantinos. 2010. Founder mutations in the ATP6V1B1 gene explain most Cypriot cases of distal renal tubular acidosis: first prenatal diagnosis. In Nephron. Clinical practice, 117, c206-12. doi:10.1159/000320192. https://pubmed.ncbi.nlm.nih.gov/20805693/
6. Boualla, L, Jdioui, W, Soulami, K, Ratbi, I, Sefiani, A. 2016. Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene. In Current research in translational medicine, 64, 5-8. doi:10.1016/j.retram.2016.01.005. https://pubmed.ncbi.nlm.nih.gov/27140593/
7. Dahmani, Malika, Talbi, Sonia, Ammar-Khodja, Fatima, Bonnet, Crystel, Petit, Christine. 2019. ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis. In International journal of pediatric otorhinolaryngology, 129, 109772. doi:10.1016/j.ijporl.2019.109772. https://pubmed.ncbi.nlm.nih.gov/31733597/
8. Han, Gwan Hee, Yun, Hee, Chung, Joon-Yong, Kim, Jae-Hoon, Cho, Hanbyoul. 2023. High ATP6V1B1 expression is associated with poor prognosis and platinum‑based chemotherapy resistance in epithelial ovarian cancer. In Oncology reports, 49, . doi:10.3892/or.2023.8539. https://pubmed.ncbi.nlm.nih.gov/36999629/