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
New TRPM6 mutation and management of hypomagnesaemia with secondary hypocalcaemia.
Katayama K et al.
Brain & Development, 2015
Kinase and channel activity of TRPM6 are co-ordinated by a dimerization motif and pocket interaction.
van der Wijst J et al.
The Biochemical Journal, 2014
Novel TRPM6 mutations in familial hypomagnesemia with secondary hypocalcemia.
Zhao Z et al.
American Journal of Nephrology, 2013
Transient receptor potential genes and human inherited disease.
Everett KV
Advances in Experimental Medicine and Biology, 2011
TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism.
Schlingmann KP et al.
Biochimica Et Biophysica Acta, 2007
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.
Schlingmann KP et al.
Journal of the American Society of Nephrology : Jasn, 2005
A critical role of TRPM channel-kinase for human magnesium transport.
Schlingmann KP et al.
The Journal of Physiology, 2005
TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption.
Voets T et al.
The Journal of Biological Chemistry, 2004
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
Schlingmann KP et al.
Nature Genetics, 2002
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