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Article

A novel Wilms' tumor 1 gene mutation in a child with severe renal dysfunction and persistent renal blastema.

Pediatric nephrology (Berlin, Germany) - 1 Sept 2008

Wagner Nicole, Wagner Kay-Dietrich, Afanetti Mickael, Nevo Fabien, Antignac Corinne, Michiels Jean-Francois, Schedl Andreas, Berard Etienne

Abstract excerpt

The Wilms' tumor suppressor gene WT1 is an important regulator of development. Mutations in this gene have been associated with Wilms' tumor, Frasier syndrome, and Denys-Drash syndrome, as well as isolated glomerular disease. Here we report the case of a 4-month-old girl, who presented with end-s...

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PMID: 18516627
DOI: 10.1007/s00467-008-0845-7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18516627-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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