Truncating <b><i>Wilms Tumor Suppressor Gene 1</i></b> Mutation in an XX Female with Adult-Onset Focal Segmental Glomerulosclerosis and Streak Ovaries: A Case Report-Reference-Cited by-同舟云学术

Truncating Wilms Tumor Suppressor Gene 1 Mutation in an XX Female with Adult-Onset Focal Segmental Glomerulosclerosis and Streak Ovaries: A Case Report

Published:2016-10-05 Issue:1 Volume:135 Page:72-76
ISSN:1660-8151
Container-title:Nephron
language:en
Short-container-title:Nephron

Author:

Hoefele Julia,Kemper Markus J.,Schoenermarck Ulf,Mueller Susanna,Klein Hanns-Georg,Lemke Anja

Publisher

S. Karger AG

Reference17 articles.

1. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients

2. A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

3. Gonadoblastoma associated with pure gonadal dysgenesis in monozygous twins

4. Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

5. Genotype–phenotype associations in WT1 glomerulopathy

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