AF350881[Secondary Source ID] - Search Results

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2002	2
2003	1
2004	1
2025	0

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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.

Walder RY, Landau D, Meyer P, Shalev H, Tsolia M, Borochowitz Z, Boettger MB, Beck GE, Englehardt RK, Carmi R, Sheffield VC. Walder RY, et al. Nat Genet. 2002 Jun;31(2):171-4. doi: 10.1038/ng901. Epub 2002 May 28. Nat Genet. 2002. PMID: 12032570

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.

Schlingmann KP, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth HW, Konrad M. Schlingmann KP, et al. Nat Genet. 2002 Jun;31(2):166-70. doi: 10.1038/ng889. Epub 2002 May 28. Nat Genet. 2002. PMID: 12032568

TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption.

Voets T, Nilius B, Hoefs S, van der Kemp AW, Droogmans G, Bindels RJ, Hoenderop JG. Voets T, et al. J Biol Chem. 2004 Jan 2;279(1):19-25. doi: 10.1074/jbc.M311201200. Epub 2003 Oct 23. J Biol Chem. 2004. PMID: 14576148 Free article.

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