Reduced FOXP3 expression causes IPEX syndrome onset: An implication from an IPEX patient and his disease-free twin brother

被引：8

作者：

Wang, Jingxue ^{[1
]}

Li, Xiaowen ^{[2
]}

Jia, Zhengcai ^{[1
]}

Tian, Yi ^{[1
]}

Yu, Jialin ^{[2
]}

Bao, Lei ^{[2
]}

Wu, Yuzhang ^{[1
]}

Ni, Bing ^{[1
]}

机构：

[1] Third Mil Med Univ, Inst Immunol, PLA, Chongqing 400038, Peoples R China

[2] Chongqing Med Univ, Childrens Hosp, Dept Neonatol, Chongqing, Peoples R China

来源：

CLINICAL IMMUNOLOGY | 2010年 / 137卷 / 01期

关键词：

FOXP3; expression; IPEX syndrome; Gene mutations; Intron; 1; IMMUNE DYSREGULATION; T-CELLS; POLYENDOCRINOPATHY; ENTEROPATHY; MUTATIONS;

D O I：

10.1016/j.clim.2010.07.006

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

引用

页码：178 / 180

页数：3

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