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Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
Schlingmann, Karl P., Weber, Stefanie, Peters, Melanie, Niemann Nejsum, Lene
, Vitzthum, Helga, Klingel, Karin, Kratz, Markus, Haddad, Elie , Ristoff, Ellinor, Dinour, Dganit, Syrrou, Maria, Nielsen, Søren, Sassen, Martin, Waldegger, Siegfried, Seyberth, Hannsjörg W. and Konrad, Martin
(2002)
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
Nature Genetics 31 (2), pp. 166-170.
Date of publication of this fulltext: 19 Dec 2024 15:42
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| Item type | Article | ||||
| Journal or Publication Title | Nature Genetics | ||||
| Publisher: | NATURE PUBLISHING GROUP | ||||
|---|---|---|---|---|---|
| Place of Publication: | NEW YORK | ||||
| Volume: | 31 | ||||
| Number of Issue or Book Chapter: | 2 | ||||
| Page Range: | pp. 166-170 | ||||
| Date | 2002 | ||||
| Institutions | Biology, Preclinical Medicine > Institut für Physiologie | ||||
| Identification Number |
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| Keywords | MAGNESIUM; EXPRESSION; PROTEIN; CHANNELS; KINASE; PARACELLIN-1; ABSORPTION; RESORPTION; TRANSPORT; CDNA; | ||||
| Dewey Decimal Classification | 500 Science > 570 Life sciences | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 72951 |
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