Associated Papers
Genetic heterogeneity in patients with Bartter syndrome type 1.
Sun M et al.
Molecular Medicine Reports, 2017
Na+-K+-2Cl- cotransporter type 2 trafficking and activity: the role of interacting proteins.
Carmosino M et al.
Biology of the Cell, 2012
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Brochard K et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2009
Dimeric architecture of the human bumetanide-sensitive Na-K-Cl Co-transporter.
Starremans PG et al.
Journal of the American Society of Nephrology : Jasn, 2003
Mutations in the human Na-K-2Cl cotransporter (NKCC2) identified in Bartter syndrome type I consistently result in nonfunctional transporters.
Starremans PG et al.
Journal of the American Society of Nephrology : Jasn, 2003
Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome.
Vargas-Poussou R et al.
American Journal of Human Genetics, 1998
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