Associated Papers
Clinical Characterization of a National Cohort of Patients With Germline WT1 Variants Including Late-Onset Phenotypes.
van Peer SE et al.
Kidney International Reports, 2024
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
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant.
Falcone MP et al.
Pediatric Nephrology (berlin, Germany), 2022
Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants.
Nagano C et al.
Kidney International Reports, 2021
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