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A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history
BACKGROUND: The EphB2 gene was recently implicated as a prostate cancer (PC) tumour suppressor gene, with somatic inactivating mutations occurring in ∼10% of sporadic tumours. We evaluated the contribution of EphB2 to inherited PC susceptibility in African Americans (AA) by screening the gene for ge...
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Hoofdauteurs: | , , , , , , , , , , , , , , , , , , , |
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Formaat: | Artigo |
Taal: | Inglês |
Gepubliceerd in: |
BMJ Group
2006
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Onderwerpen: | |
Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2564535/ https://ncbi.nlm.nih.gov/pubmed/16155194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.035790 |
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