Deletion of claudin-10 rescues claudin-16–deficient mice from hypomagnesemia and hypercalciuria

Author:

Breiderhoff Tilman,Himmerkus Nina,Drewell Hoora,Plain Allein,Günzel Dorothee,Mutig Kerim,Willnow Thomas E.,Müller Dominik,Bleich Markus

Publisher

Elsevier BV

Subject

Nephrology

Reference33 articles.

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3. Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis;Weber;J Am Soc Nephrol,2001

4. A novel hypokalemic-alkalotic salt-losing tubulopathy in patients with CLDN10 mutations [e-pub ahead of print];Bongers;J Am Soc Nephrol,2015

5. Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage;Klar;PLoS Genet,2017

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