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Prevalence of deleterious mutations among patients with breast cancer referred for multigene panel testing in a Romanian population

机译:在罗马尼亚人口中接受多基因面板测试的乳腺癌患者中有害突变的患病率

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摘要

AimMultigene panel testing for Hereditary Breast and Ovarian Cancer (HBOC) using next generation sequencing is becoming more common in medical care.We report our experience regarding deleterious mutations of high and moderate-risk breast cancer genes (BRCA1/2, TP53, STK11, CDH1, PTEN, PALB2, CHEK2, ATM), as well as more recently identified cancer genes, many of which have increased risk but less well-defined penetrance.
机译:AimMultigene小组使用下一代测序对遗传性乳腺癌和卵巢癌(HBOC)进行的检测在医疗保健中变得越来越普遍。我们报告了我们对高风险和中风险乳腺癌基因(BRCA1 / 2,TP53,STK11,CDH1的有害突变)的经验,PTEN,PALB2,CHEK2,ATM),以及最近发现的癌症基因,其中许多基因具有增加的风险,但外显率较低。

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