New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia

CNNM2, Encoding a Basolateral Protein Required for Renal Mg2+ Handling, Is Mutated in Dominant Hypomagnesemia

(2011) Marchel Stuiver et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Role of the Transient Receptor Potential Vanilloid 5 (TRPV5) Protein N Terminus in Channel Activity, Tetramerization, and Trafficking

(2011) Theun de Groot et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes

(2011) T. Guran et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Novel molecular pathways in renal Mg2+ transport: a guided tour along the nephron

(2010) Pedro San-Cristobal et al.   CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION

Transient Receptor Potential Melastatin 6 Knockout Mice Are Lethal whereas Heterozygous Deletion Results in Mild Hypomagnesemia

(2010) Titia E. Woudenberg-Vrenken et al.   NEPHRON PHYSIOLOGY

Mice defective in Trpm6 show embryonic mortality and neural tube defects

(2009) R. Y. Walder et al.   HUMAN MOLECULAR GENETICS

Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutation

(2008) Dolors Esteban-Oliva et al.   EUROPEAN JOURNAL OF PEDIATRICS

A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation

(2008) Hursit Apa et al.   INDIAN JOURNAL OF PEDIATRICS

Proinflammatory Mediators Modulate the Heat-Activated Ion Channel TRPV1 via the Scaffolding Protein AKAP79/150

(2008) Xuming Zhang et al.   NEURON