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Association of PALB2 sequence variants with the risk of familial and early-onset breast cancer in a South-American population
BACKGROUND: Germline mutations in PALB2 have been identified in approximately 1% of familial breast cancer (BC) in several populations. Nevertheless its contribution in the South-American population is unknown. The goal of this study was to determine the prevalence of PALB2 mutations in the Chilean...
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| Veröffentlicht in: | BMC Cancer |
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| Hauptverfasser: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4323211/ https://ncbi.nlm.nih.gov/pubmed/25636233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-015-1033-3 |
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