Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Background and objectives: The risk of developing Wilms tumor (WT) can be present or absent in patients with nephrotic syndrome (NS) caused by WT1 mutations. Here, the genotype/phenotype correlation regarding the outcome and risk for WT in 52 patients from 51 families with NS due to WT1 mutations is...

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Detalhes bibliográficos
Main Authors: Chernin, Gil, Vega-Warner, Virginia, Schoeb, Dominik S., Heeringa, Saskia F., Ovunc, Bugsu, Saisawat, Pawaree, Cleper, Roxana, Ozaltin, Fatih, Hildebrandt, Friedhelm
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2010
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2974408/
https://ncbi.nlm.nih.gov/pubmed/20595692
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.09351209
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