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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265448/ https://www.ncbi.nlm.nih.gov/pubmed/25466287 http://dx.doi.org/10.1186/1471-2407-14-902 |