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NDT Advance Access published online on April 6, 2005
Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfh799
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© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org
Received May 28, 2004
Accepted February 15, 2005

Case Report

CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease

Nesrin Besbas 1*, Fatih Ozaltin 1, Nikola Jeck 2, Hannsjörg Seyberth 2, and Michael Ludwig 3

1 Department of Pediatrics, Unit of Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey
2 Department of Pediatrics, Philipps University of Marburg, Germany
3 Department of Clinical Biochemistry, University of Bonn, Bonn, Germany

* To whom correspondence should be addressed.
Nesrin Besbas, E-mail: nbesbas{at}hacettepe.edu.tr



This article has no Abstract. Keywords: chloride channel 5 (ClC-5); CLCN5 gene; Dent's disease; metabolic alkalosis.
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