1. Chiang, Han-Sun, Wang, Ya-Yun, Lin, Ying-Hung, Wu, Yi-No. 2019. The role of SLC9A3 in Taiwanese patients with congenital bilateral absence of vas deferens (CBAVD). In Journal of the Formosan Medical Association = Taiwan yi zhi, 118, 1576-1583. doi:10.1016/j.jfma.2019.01.019. https://pubmed.ncbi.nlm.nih.gov/30797621/
2. Chen, Kuo-Chiang, Chang, Meng-Lin, Lin, Chun-Sian, Maa, Hung-Chune, Wu, Yi-No. 2023. Insight into SLC9A3 deficiency-mediated micturition dysfunction caused by electrolyte imbalance. In Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 158, 114155. doi:10.1016/j.biopha.2022.114155. https://pubmed.ncbi.nlm.nih.gov/36916397/
3. Wang, Ya-Yun, Lin, Ying-Hung, Wu, Yi-No, Cheng, Chiao-Yin, Chiang, Han-Sun. 2017. Loss of SLC9A3 decreases CFTR protein and causes obstructed azoospermia in mice. In PLoS genetics, 13, e1006715. doi:10.1371/journal.pgen.1006715. https://pubmed.ncbi.nlm.nih.gov/28384194/
4. Dimitrov, Georges, Bamberger, Sarah, Navard, Chloe, Hugot, Jean-Pierre, Fabre, Alexandre. 2019. Congenital Sodium Diarrhea by mutation of the SLC9A3 gene. In European journal of medical genetics, 62, 103712. doi:10.1016/j.ejmg.2019.103712. https://pubmed.ncbi.nlm.nih.gov/31276831/
5. Dorfman, Ruslan, Taylor, Chelsea, Lin, Fan, Durie, Peter, Zielenski, Julian. 2010. Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis. In Pediatric pulmonology, 46, 385-92. doi:10.1002/ppul.21372. https://pubmed.ncbi.nlm.nih.gov/20967843/
6. Bogdanic, Ema, Müller, Thomas, Heinz-Erian, Peter, Janecke, Andreas R, Rückel, Aline. 2022. Further delineation of SLC9A3-related congenital sodium diarrhea. In Molecular genetics & genomic medicine, 10, e2000. doi:10.1002/mgg3.2000. https://pubmed.ncbi.nlm.nih.gov/35775128/