Hussein, Mahmoud Al, Shafiqa Saleh, Sura El Doory, Mohammed Ali Al Sabbah, and Maysa Saleh. “TRPM6 Gene Mutation Responsible for Familial Hypomagnesemia With Secondary Hypocalcemia”. Archives of Clinical and Medical Case Reports 3, no. 1 (January 22, 2019): 23–26. Accessed June 15, 2026. https://fortunejournals.org/ojs/index.php/acmcr/article/view/22117.