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Absence of truncating BRIP1 mutations in chromosome 17q-linked hereditary prostate cancer families
BACKGROUND: In a genome-wide scan (GWS) of 175 multiplex prostate cancer (PCa) families from the University of Michigan Prostate Cancer Genetics Project (PCGP), linkage was observed to markers on chromosome 17q21–24, a region that includes two breast cancer susceptibility genes, BRCA1 and BRIP1. BRI...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2795448/ https://ncbi.nlm.nih.gov/pubmed/19935797 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjc.6605433 |
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