CDH1
先证者
癌症
遗传学
分子遗传学
突变
基因
种系突变
遗传倾向
医学
生物
细胞
钙粘蛋白
作者
Tsukanov Ac,Yu. A. Shelygin,Kashnikov Vn,Frolov Sa,Liubchenko Ln,В. П. Шубин,Karpukhin Av,Muzaffarova Ta,Н. И. Поспехова
出处
期刊:PubMed
日期:2013-01-01
卷期号:59 (5): 580-4
被引量:1
摘要
About 3% of cases of gastric cancer (GC) cases are due to hereditary predisposition. Molecular causes of inherited predisposition to diffuse GC among Russian patients have not been studied. In the present work there was performed the molecular genetics study in 9 probands with signet-ring cell GC. Search of hereditary mutations was conducted in a suppressor gene of diffuse GC - the gene CDH1. We have discovered a new hereditary mutation (c.1005delA) and one rare variant (s.2253C> T). Frequency of hereditary mutations in sample of patients Russian was 1/9 (11,1%).
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