Familial Hypomagnesemia with Secondary Hypocalcaemia Due to TRPM6 Gene Mutation in A Pediatric Patient. Journal of Bangladesh College of Physicians and Surgeons, [S. l.], v. 44, n. 2, p. 135–137, 2026. DOI: 10.3329/jbcps.v44i2.89348. Disponível em: https://www.banglajol.info/index.php/JBCPS/article/view/89348. Acesso em: 2 jul. 2026.