HOME > 新闻 > 详情

TBX6基因多态性与先天性脊柱侧凸相关

2018-04-10 17:38:41

The single SNP analysis showed allele frequency of rs2289292 (exon 8, the only tagging SNP) and rs3809624 (5’untranslated region) demonstrated significant difference between CS cases and controls (P = 0.017 and P = 0.033),which suggests genetic variants of TBX6 gene is associated with CS.

Last:TBX6基因罕见突变联合常见亚效等位基因导致先天性脊柱侧凸的遗传学模型

Next:GPR126在青少年特发性脊柱侧凸中基因多态性及PUMC分型关联性研究

中国医学科学院,北京协和医学院,北京协和医院骨科,北京,中国

骨骼畸形遗传学研究北京市重点实验室

中国医学科学院,骨科医学研究中心

电话: +86-10-69152809

电子邮件: dr.wunan@pumch.cn

地址: 北京市东城区帅府园1号,北京协和医院骨科,100730

Welcome to Deciphering Disorders Involving Scoliosis and COmorbidities,

Copyright © 2018 DISCO. All Rights Reserved.