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Pathologic Outcomes Associated with the 17q Prostate Cancer Risk Variants
PURPOSE: Recent studies have identified 2 distinct genetic variants along chromosome 17 (allele T of SNP rs4430796 on 17q12 and allele G of SNP rs1859962 on 17q24) that have been linked to prostate cancer (CaP) risk. Less is known about tumor pathology features in carriers of these variants. MATERIA...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3140699/ https://ncbi.nlm.nih.gov/pubmed/19371897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.juro.2009.01.109 |
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