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Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example
Only approximately 50% of all familial breast cancers can be explained by known genetic factors, including mutations in BRCA1 and BRCA2. One of the most extensively studied candidates for breast and/or ovarian cancer susceptibility is BARD1. Although it was suggested that large mutations may contrib...
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| Publicado no: | Sci Rep |
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| Principais autores: | , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4439969/ https://ncbi.nlm.nih.gov/pubmed/25994375 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep10424 |
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