Associated Papers
Pathogenic variants prevalence patients with diabetic kidney disease in Japan: A descriptive study.
Hashiba T et al.
Journal of Diabetes Investigation, 2025
High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.
Smith C et al.
Kidney International Reports, 2023
37850022 (PubMed )
Supplement: mmc1.pdf
Genotype-phenotype correlation of WT1 mutation-related nephropathy in Chinese children.
Chen H et al.
Frontiers in Pediatrics, 2023
Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants.
Nagano C et al.
Kidney International Reports, 2021
34386660 (PubMed )
Supplement: mmc1.pdf
A novel WT1 gene mutation in a chinese girl with denys-drash syndrome.
Wang F et al.
Journal of Clinical Laboratory Analysis, 2021
Wilms tumor gene single nucleotide polymorphism rs16754 predicts a favorable outcome in children with acute lymphoblastic leukemia.
Junghanns AS et al.
Journal of Cancer Research and Clinical Oncology, 2015
Genotype-phenotype associations in WT1 glomerulopathy.
Lipska BS et al.
Kidney International, 2014
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