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Article

WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Apr 2003

Loirat Chantal, André Jean Luc, Champigneulle Jacqueline, Acquaviva Cécile, Chantereau Dominique, Bourquard Rosine, Elion Jacques, Denamur Erick

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PMID: 12637656
DOI: 10.1093/ndt/gfg041

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WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour.PMID 12637656Read ↗

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WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia.Semantic proximity Read ↗

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.Semantic proximity Read ↗

WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.Semantic proximity Read ↗

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes.Semantic proximity Read ↗

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.Semantic proximity Read ↗

46,XY phenotypic male with focal segmental glomerulosclerosis caused by the WT1 splice site mutation.Semantic proximity Read ↗

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