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NDT Advance Access published online on November 22, 2005
Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfi285
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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@oxfordjournals.org
Received August 10, 2005
Accepted November 3, 2005

Case Report

A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy

Valérie Schumacher 1, Julia Thumfart 2, Matthias Drechsler 1, Maximillian Essayie 3, Brigitte Royer-Pokora 1, Uwe Querfeld 2, and Dominik Müller 2 *

1 Institute of Human Genetics, Heinrich-Heine University Düsseldorf, Germany
2 Department of Pediatric Nephrology, Charité Children's Hospital Berlin, Germany
3 Department of Pediatric Endocrinology, Charité Children's Hospital Berlin, Germany

* To whom correspondence should be addressed.
Dominik Müller, E-mail: dominik.mueller{at}charite.de



This article has no Abstract. Keywords: cortical atrophy; Denys-Drash syndrome; WT1 mutation.
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