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The Journal of Membrane Biology|October 30, 2009
FXYD2 and Na,K-ATPase expression in isolated human proximal tubular cells: disturbed upregulation on renal hypomagnesemia?Edinio R Cairo, Herman G P Swarts, Martijn J G Wilmer, et al.Biochimica Et Biophysica Acta|November 6, 2007
Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemiaEdinio R Cairo, Thomas Friedrich, Herman G P Swarts, et al.American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.European Journal of Human Genetics : EJHG|August 21, 2014
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraineSe-Kyung Oh, Jeong-In Baek, Karl M Weigand, et al.Pageof 3