Ontology highlight
ABSTRACT:
SUBMITTER: Liao D
PROVIDER: S-EPMC4397537 | biostudies-literature | 2015 Apr
REPOSITORIES: biostudies-literature
Liao Dan D Hou Shengping S Zhang Jun J Fang Jing J Liu Yunjia Y Bai Lin L Cao Qingfeng Q Kijlstra Aize A Yang Peizeng P
Scientific reports 20150415
This study aimed to investigate the role of genetic variants including single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) of TBX21, GATA3, Rorc and Foxp3 genes in Behcet's disease (BD) and Vogt-Koyanagi-Harada (VKH) syndrome in a Chinese Han population. Genotyping of 25 SNPs was performed by iPLEX system (Sequenom) or polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). TaqMan real time PCR was used to assess CNVs. The expression of Rorc and Foxp3 we ...[more]