A point mutation found in the WT1 gene in a sporadic Wilms’ tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys-Drash syndrome.

AKASAKA Y; KIKUCHI H; NAGAI T; HIRAOKA N; KATO S; HATA J

Art

J-GLOBAL ID：200902172041467816 Reference number：93A0249424

A point mutation found in the WT1 gene in a sporadic Wilms’ tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys-Drash syndrome.

尿生殖器の正常な散発性Wilms腫ようのWT1遺伝子で発見した点突然変異はDenys-Drash症候群の最高頻度の点突然変異と同一である

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Author (6)： , , , , ,
Material：
Volume： 317 Issue： 1/2 Page： 39-43 Publication year： Feb. 08, 1993
JST Material Number： D0575A ISSN： 0014-5793 Document type： Article
Article type：原著論文 Country of issue： United States (USA) Language： ENGLISH (EN)

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Genetic variation , Congenital diseases,deformities in general. , Basic medicine on urogenital system

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