Novel Familial WT1 Read-Through Mutation Associated With Wilms Tumor and Slow Progressive Nephropathy
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference14 articles.
1. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms’ tumor locus;Call;Cell,1990
2. Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping;Gessler;Nature,1990
3. Familial Wilms tumor;Ruteshouser;Am J Med Genet,2004
4. Wilms tumor genetics;Huff;Am J Med Genet,1998
5. Infrequent mutation of the WT1 gene in 77 Wilms’ tumors;Gessler;Hum Mutat,1994
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