Article
Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia.
Proceedings of the National Academy of Sciences of the United States of America - 2 Mar 2004
Chubanov Vladimir, Waldegger Siegfried, Mederos y Schnitzler Michael, Vitzthum Helga, Sassen Martin C, Seyberth Hannsjörg W, Konrad Martin, Gudermann Thomas
Abstract excerpt
Impaired magnesium reabsorption in patients with TRPM6 gene mutations stresses an important role of TRPM6 (melastatin-related TRP cation channel) in epithelial magnesium transport. While attempting to isolate full-length TRPM6, we found that the human TRPM6 gene encodes multiple mRNA isoforms. Fu...
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