A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family. Iranian Journal of Kidney Diseases, [S. l.], v. 16, n. 3, p. 209–213, 2022. Disponível em: https://ijkd.org/index.php/ijkd/article/view/6845. Acesso em: 5 jul. 2025.