Associated Papers
The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study.
Zhu X et al.
Frontiers in Medicine, 2022
35755072 (PubMed )
Supplement: Data_Sheet_1.PDF
Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome.
Yang Y et al.
Genetics and Molecular Research : Gmr, 2016
Bilateral Wilms tumor and early presentation in pediatric patients is associated with the truncation of the Wilms tumor 1 protein.
Hu M et al.
The Journal of Pediatrics, 2013
Discordant phenotypes in monozygotic twins with identical de novo WT1 mutation.
Yu Z et al.
Clinical Kidney Journal, 2012
Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.
Mucha B et al.
Pediatric Research, 2006
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