HUSSEIN, Mahmoud Al; SALEH, Shafiqa; DOORY, Sura El; SABBAH, Mohammed Ali Al; SALEH, Maysa. TRPM6 Gene Mutation Responsible for Familial Hypomagnesemia with Secondary Hypocalcemia. Archives of Clinical and Medical Case Reports, [S. l.], v. 3, n. 1, p. 23–26, 2019. Disponível em: https://fortunejournals.org/ojs/index.php/acmcr/article/view/22117. Acesso em: 15 jun. 2026.