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Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer
BACKGROUND: Using a genome-wide approach, we have previously observed an increase in the frequency of rare copy number variants (CNVs) in familial and early-onset breast cancer cases when compared to controls. Moreover, the biological networks of the CNV disrupted genes differed between the two grou...
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| Publicado no: | BMC Cancer |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4265448/ https://ncbi.nlm.nih.gov/pubmed/25466287 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2407-14-902 |
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