Authors
Hanna Rennert, Dani Bercovich, Ayala Hubert, Dvora Abeliovich, Uri Rozovsky, Anat Bar-Shira, Sonya Soloviov, Letizia Schreiber, Haim Matzkin, Gad Rennert, Luna Kadouri, Tamar Peretz, Yuval Yaron, Avi Orr-Urtreger
Publication date
2002/10/1
Journal
The American Journal of Human Genetics
Volume
71
Issue
4
Pages
981-984
Publisher
Elsevier
Description
HPC1/RNASEL was recently identified as a candidate gene for hereditary prostate cancer. We identified a novel founder frameshift mutation in RNASEL, 471delAAAG, in Ashkenazi Jews. The mutation frequency in the Ashkenazi population, estimated on the basis of the frequency in 150 healthy young women, was 4% (95% confidence interval [CI] 1.9%–8.4%). Among Ashkenazi Jews, the mutation frequency was higher in patients with prostate cancer (PRCA) than in elderly male control individuals (6.9% vs. 2.4%; odds ratio=3.0; 95% CI 0.6–15.3; P=.17). 471delAAAG was not detected in the 134 non-Ashkenazi patients with PRCA and control individuals tested. The median age at PRCA diagnosis did not differ significantly between the Ashkenazi carriers and noncarriers included in our study. However, carriers received diagnoses at a significantly earlier age, compared with patients with PRCA who were …
Total citations
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