乳腺癌
医学
基因检测
遗传学
肿瘤科
癌症
内科学
生物
作者
Parvin Rostami,Kazem Zendehdel,Reza Shirkoohi,Elmira Ebrahimi,Mitra Ataei,Hashem Imanian,Hossein Najmabadi,Mohammad R. Akbari,Mohammad Hossein Sanati
出处
期刊:PubMed
日期:2020-03-01
卷期号:23 (3): 155-162
被引量:10
摘要
Breast cancer (BC) is a highly complex, heterogeneous and multifactorial disease and is the most commonly diagnosed cancer and the leading cause of cancer-related mortality in women worldwide. Family history and genetic mutations are important risk factors for BC. While studies in twins have estimated that about 10%-30% of BC are due to hereditary factors, only 4%-5% of them are due to mutations in BRCA1 or BRCA2 genes. Our aim was to investigate the role of other BC genes in familial BC among the Iranian population.
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