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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Главные авторы: Xuan, Dennis, Li, Guoliang, Cai, Qiuyin, Deming-Halverson, Sandra, Shrubsole, Martha J., Shu, Xiao-Ou, Kelley, Mark C., Zheng, Wei, Long, Jirong
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2013
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Online-ссылка: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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