Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database-Reference-Cited by-同舟云学术

Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database

Published:1998-04 Issue:4 Volume:62 Page:824-833
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Jeanpierre C.,Denamur E.,Henry I.,Cabanis M.-O.,Luce S.,Cécille A.,Elion J.,Peuchmaur M.,Loirat C.,Niaudet P.,Gubler M.-C.,Junien C.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference42 articles.

1. 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;FEBS Lett,1993

2. Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome;Baird;Hum Mol Genet,1992

3. Donor splice-site mutations in WT1 are responsible for Frasier syndrome;Barbaux;Nat Genet,1997

4. WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion;Bardeesy;Genomics,1994

5. Tying all together: epigenetics, genetics, cell cycle and cancer;Baylin;Science,1997

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