1. Rouka, Erasmia, Liakopoulos, Vassilios, Gourgoulianis, Konstantinos I, Hatzoglou, Chrissi, Zarogiannis, Sotirios G. 2019. In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria. In Medicina (Kaunas, Lithuania), 55, . doi:10.3390/medicina55080409. https://pubmed.ncbi.nlm.nih.gov/31357502/
2. Kuo, Shou-Jen, Chien, Su-Yu, Lin, Che, Tsai, Hsiu-Ting, Chen, Dar-Ren. . Significant elevation of CLDN16 and HAPLN3 gene expression in human breast cancer. In Oncology reports, 24, 759-66. doi:. https://pubmed.ncbi.nlm.nih.gov/20664984/
3. Malakoutian, Tahereh, Madadi, Bahareh, Saber, Siamak. . A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family. In Iranian journal of kidney diseases, 16, 209-213. doi:. https://pubmed.ncbi.nlm.nih.gov/35714216/
4. Radonsky, Vanessa, Kizys, Marina Malta Letro, Dotto, Renata Pires, Dias-da-Silva, Magnus Regios, Lazaretti-Castro, Marise. 2020. Hypomagnesemia with Hypercalciuria Leading to Nephrocalcinosis, Amelogenesis Imperfecta, and Short Stature in a Child Carrying a Homozygous Deletion in the CLDN16 Gene. In Calcified tissue international, 107, 403-408. doi:10.1007/s00223-020-00726-y. https://pubmed.ncbi.nlm.nih.gov/32710267/
5. Hanssen, Oriane, Castermans, Emilie, Bovy, Christophe, Krzesinski, Jean-Marie, Jouret, François. 2014. Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosis. In Clinical kidney journal, 7, 282-5. doi:10.1093/ckj/sfu019. https://pubmed.ncbi.nlm.nih.gov/25852890/
6. Yamaguti, Paulo Marcio, dos Santos, Pollyanna Almeida Costa, Leal, Bruno Sakamoto, Acevedo, Ana Carolina, Neves, Francisco de Assis Rocha. 2015. Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report. In BMC nephrology, 16, 92. doi:10.1186/s12882-015-0079-4. https://pubmed.ncbi.nlm.nih.gov/26136118/
7. Zhang, Hejia, Ling, Chen, Liu, Xiaorong. . A novel CLDN16 mutation in familial hypomagnesemia with hypercalciuria and nephrocalcinosis
. In Clinical nephrology, 92, 95-97. doi:10.5414/CN109637. https://pubmed.ncbi.nlm.nih.gov/31232269/