Associated Papers
Single-cell transcriptomics identifies aberrant glomerular angiogenic signalling in the early stages of WT1 kidney disease.
Chandler JC et al.
The Journal of Pathology, 2024
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant.
Falcone MP et al.
Pediatric Nephrology (berlin, Germany), 2022
A novel mutation of WT1 exon 9 in a patient with Denys-Drash syndrome and pyloric stenosis.
Hu M et al.
Pediatric Nephrology (berlin, Germany), 2004
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