1. Karakilic-Ozturan, E, Ozturk, A P, Oney, C, Bas, F, Darendeliler, F. . SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS. In Acta endocrinologica (Bucharest, Romania : 2005), 18, 387-391. doi:10.4183/aeb.2022.387. https://pubmed.ncbi.nlm.nih.gov/36699160/
2. Sadeghi-Alavijeh, Omid, Chan, Melanie M Y, Moochhala, Shabbir H, Gale, Daniel P, Böckenhauer, Detlef. 2023. Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease. In Kidney international, 104, 975-984. doi:10.1016/j.kint.2023.06.019. https://pubmed.ncbi.nlm.nih.gov/37414395/
3. Ichikawa, Shoji, Sorenson, Andrea H, Imel, Erik A, Gertner, Joseph M, Econs, Michael J. 2006. Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria. In The Journal of clinical endocrinology and metabolism, 91, 4022-7. doi:. https://pubmed.ncbi.nlm.nih.gov/16849419/
4. Zhu, Zewu, Bo-Ran Ho, Bryan, Chen, Alyssa, Deng, Yanhong, Bergwitz, Clemens. 2024. An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH). In Kidney international, 105, 1058-1076. doi:10.1016/j.kint.2024.01.031. https://pubmed.ncbi.nlm.nih.gov/38364990/
5. Stürznickel, Julian, Heider, Fiona, Delsmann, Alena, Amling, Michael, Oheim, Ralf. 2022. Clinical Spectrum of Hereditary Hypophosphatemic Rickets With Hypercalciuria (HHRH). In Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 37, 1580-1591. doi:10.1002/jbmr.4630. https://pubmed.ncbi.nlm.nih.gov/35689455/
6. Molin, Arnaud, Lemoine, Sandrine, Kaufmann, Martin, Bacchetta, Justine, Kottler, Marie-Laure. 2021. Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. In Frontiers in endocrinology, 12, 736240. doi:10.3389/fendo.2021.736240. https://pubmed.ncbi.nlm.nih.gov/34721296/