1. Schlingmann, Karl P, Ruminska, Justyna, Kaufmann, Martin, Wagner, Carsten A, Konrad, Martin. 2015. Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia. In Journal of the American Society of Nephrology : JASN, 27, 604-14. doi:10.1681/ASN.2014101025. https://pubmed.ncbi.nlm.nih.gov/26047794/
2. Giusti, Francesca, Marini, Francesca, Al-Alwani, Hatim, Khan, Aliya A, Brandi, Maria Luisa. 2023. A Novel Heterozygous Mutation c.1627G>T (p.Gly543Cys) in the SLC34A1 Gene in a Male Patient with Recurrent Nephrolithiasis and Early Onset Osteopenia: A Case Report. In International journal of molecular sciences, 24, . doi:10.3390/ijms242417289. https://pubmed.ncbi.nlm.nih.gov/38139117/
3. De Paolis, Elisa, Scaglione, Giovanni Luca, De Bonis, Maria, Minucci, Angelo, Capoluongo, Ettore. . CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype. In Clinical chemistry and laboratory medicine, 57, 1650-1667. doi:10.1515/cclm-2018-1208. https://pubmed.ncbi.nlm.nih.gov/31188746/
4. Kurnaz, Erdal, Savaş Erdeve, Şenay, Çetinkaya, Semra, Aycan, Zehra. 2018. Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene. In Hormone research in paediatrics, 91, 278-284. doi:10.1159/000492899. https://pubmed.ncbi.nlm.nih.gov/30227399/
5. Geraghty, Robert, Lovegrove, Catherine, Howles, Sarah, Sayer, John A. 2024. Role of Genetic Testing in Kidney Stone Disease: A Narrative Review. In Current urology reports, 25, 311-323. doi:10.1007/s11934-024-01225-5. https://pubmed.ncbi.nlm.nih.gov/39096463/
6. Carlile, Mark, Swan, Daniel, Jackson, Kelly, Flicek, Paul, Werner, Andreas. 2009. Strand selective generation of endo-siRNAs from the Na/phosphate transporter gene Slc34a1 in murine tissues. In Nucleic acids research, 37, 2274-82. doi:10.1093/nar/gkp088. https://pubmed.ncbi.nlm.nih.gov/19237395/
7. Qiu, Jiechuan, Wang, Zicheng, Xu, Yingkun, Wang, Qingliang, Xia, Qinghua. 2023. Low expression of SLC34A1 is associated with poor prognosis in clear cell renal cell carcinoma. In BMC urology, 23, 45. doi:10.1186/s12894-023-01212-x. https://pubmed.ncbi.nlm.nih.gov/36978048/
8. 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/
9. Wang, Qiao, Chen, Jia-Jia, Wei, Li-Ya, Su, Chang, Gong, Chun-Xiu. 2024. Biallelic and monoallelic pathogenic variants in CYP24A1 and SLC34A1 genes cause idiopathic infantile hypercalcemia. In Orphanet journal of rare diseases, 19, 126. doi:10.1186/s13023-024-03135-8. https://pubmed.ncbi.nlm.nih.gov/38504242/
10. 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/
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