Lataa...
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...
Tallennettuna:
| Julkaisussa: | BMC Cancer |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2014
|
| Aiheet: | |
| Linkit: | 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 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|