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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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Détails bibliographiques
Auteurs principaux: Helfand, Brian T., Loeb, Stacy, Meeks, Joshua J., Fought, Angela J., Kan, Donghui, Catalona, William J.
Format: Artigo
Langue:Inglês
Publié: 2009
Sujets:
Accès en ligne: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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