1 | FXYGD2, HOMG2
|
| Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemia.
|
| Cairo ER, Friedrich T, Swarts HG, Knoers NV, Bindels RJ, Monnens LA, Willems PH, De Pont JJ, Koenderink JB.
|
| Biochim Biophys Acta 1778(2):398-404. Epub 2007 Oct 17.PMID: 17980699 2008
|
2 | HOMG2
|
| Genetic heterogeneity in familial renal magnesium wasting.
|
| Kantorovich V, Adams JS, Gaines JE, Guo X, Pandian MR, Cohn DH, Rude RK.
|
| J Clin Endocrinol Metab 87(2):612-7. 2002
|
3 | HOMG2
|
| Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit.
|
| Meij IC, Koenderink JB, van Bokhoven H, Assink KF, Groenestege WT, de Pont JJ, Bindels RJ, Monnens LA, van den Heuvel LP, Knoers NV.
|
| Nat Genet 26(3):265-6. 2000
|
4 | HOMG2
|
| Hereditary isolated renal magnesium loss maps to chromosome 11q23.
|
| Meij IC, et al.
|
| Am J Hum Genet 64 : 180-188. 1999
|