Citations for
1FXYGD2, 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
2HOMG2
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
3HOMG2
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
4HOMG2
Hereditary isolated renal magnesium loss maps to chromosome 11q23.
Meij IC, et al.
Am J Hum Genet 64 : 180-188. 1999