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- W4245002918 endingPage "274" @default.
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- W4245002918 abstract "The WT1 gene, located at 11p13, encodes a zinc finger transcription factor involved in renal and gonadal development and in Wilms' tumor. Constitutional mutations of this gene have been described in most patients with Denys Drash syndrome (mesangial sclerosis associated with male pseudohermaphrodism and/or Wilms' tumor), but also in patients with genitourinary abnormalities and Wilms' tumor (WT) or presenting with only unilateral or bilateral WT. Moreover, ∼10% of Wilms' tumors carry WT1 mutations at the somatic level. To facilitate the genotype-phenotype correlation analyses, we have created a software package along with a computerized database of germline (70 entries) and somatic (28 entries) mutations reported in the literature." @default.
- W4245002918 created "2022-05-12" @default.
- W4245002918 creator A5075676296 @default.
- W4245002918 date "1998-01-01" @default.
- W4245002918 modified "2023-10-18" @default.
- W4245002918 title "Software and database for the analysis of mutations in the human WT1 gene" @default.
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- W4245002918 doi "https://doi.org/10.1093/nar/26.1.271" @default.
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