26 March 2024 : Case report
A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant
Challenging differential diagnosis, Management of emergency care, Rare disease, Congenital defects / diseases
DOI: 10.12659/AJCR.942498
Am J Case Rep 2024; 25:e942498