bibliographicCitation |
Sha Q, Pearson W, Burcea LC, Wigfall DA, Schlesinger PH, Nichols CG, Mercer RW. Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel. American Journal of Physiology-Renal Physiology. 2008 Jul;295(1):F91–9. doi: 10.1152/ajprenal.00519.2007. |