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Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

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. Full-...

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Bibliografiske detaljer
Main Authors: Chubanov, Vladimir, Waldegger, Siegfried, Schnitzler, Michael Mederos y, Vitzthum, Helga, Sassen, Martin C., Seyberth, Hannsjörg W., Konrad, Martin, Gudermann, Thomas
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 2004
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC365716/
https://ncbi.nlm.nih.gov/pubmed/14976260
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0305252101
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