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Discovery of rare coding variants in OGDHL and BRCA2 in relation to breast cancer risk in Chinese women

The missing heritability of breast cancer could be partially attributed to rare variants (MAF < 0.5%). To identify breast cancer-associated rare coding variants, we conducted whole-exome sequencing (~50×) in genomic DNA samples obtained from 831 breast cancer cases and 839 controls of Chinese fem...

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Detalhes bibliográficos
Publicado no:Int J Cancer
Principais autores: Guo, Xingyi, Long, Jirong, Chen, Zhishan, Shu, Xiao-ou, Xiang, Yong-Bing, Wen, Wanqing, Zeng, Chenjie, Gao, Yu-Tang, Cai, Qiuyin, Zheng, Wei
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7453427/
https://ncbi.nlm.nih.gov/pubmed/31837001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ijc.32825
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