Associated Papers
Case Report: Novel TRPM6 Mutations Cause Hereditary Hypomagnesemia With Secondary Hypocalcemia in a Chinese Family and a Literature Review.
Han Y et al.
Frontiers in Pediatrics, 2022
Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6.
Astor MC et al.
Endocrine Connections, 2015
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