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APOBEC3 deletion polymorphism is associated with breast cancer risk among women of European ancestry
Copy number variations occur frequently in the genome and are a significant source of human genetic variation accounting for disease. Recently, we discovered a common deletion located in the APOBEC3A and APOBEC3B genes significantly associated with breast cancer in Chinese women. Investigating this...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3786378/ https://ncbi.nlm.nih.gov/pubmed/23715497 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/carcin/bgt185 |
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