Late-Onset Manifestation of Antenatal Bartter Syndrome as a Result of Residual Function of the Mutated Renal Na+-K+-2Cl−Co-Transporter-Reference-Cited by-同舟云学术

Late-Onset Manifestation of Antenatal Bartter Syndrome as a Result of Residual Function of the Mutated Renal Na+-K+-2Cl−Co-Transporter

Published:2006-06-28 Issue:8 Volume:17 Page:2136-2142
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Pressler Carsten A.,Heinzinger Jolanta,Jeck Nikola,Waldegger Petra,Pechmann Ulla,Reinalter Stephan,Konrad Martin,Beetz Rolf,Seyberth Hannsjörg W.,Waldegger Siegfried

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference15 articles.

1. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2

2. Salt handling in the distal nephron: lessons learned from inherited human disorders

3. Mutations in the Human Na-K-2Cl Cotransporter (NKCC2) Identified in Bartter Syndrome Type I Consistently Result in Nonfunctional Transporters

4. Impaired response to furosemide in hyperprostaglandin E syndrome: Evidence for a tubular defect in the loop of Henle

5. A New ER Trafficking Signal Regulates the Subunit Stoichiometry of Plasma Membrane KATP Channels

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