A refined study of FCRL genes from a genome-wide association study for Graves' disease.

A refined study of FCRL genes from a genome-wide association study for Graves' disease.

To pinpoint the exact location of the etiological variant/s present at 1q21.1 harboring FCRL1-5 and CD5L genes, we carried out a refined association study in the entire FCRL region in 1,536 patients with Graves' disease (GD) and 1,516 sex-matched controls by imputation analysis, logistic regres...

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Bibliographic Details
Main Authors:	Shuang-Xia Zhao, Wei Liu, Ming Zhan, Zhi-Yi Song, Shao-Ying Yang, Li-Qiong Xue, Chun-Ming Pan, Zhao-Hui Gu, Bing-Li Liu, Hai-Ning Wang, Liming Liang, Jun Liang, Xiao-Mei Zhang, Guo-Yue Yuan, Chang-Gui Li, Ming-Dao Chen, Jia-Lun Chen, Guan-Qi Gao, Huai-Dong Song, China Consortium for the Genetics of Autoimmune Thyroid Disease
Format:	Article
Language:	English
Published:	Public Library of Science (PLoS) 2013-01-01
Series:	PLoS ONE
Online Access:	http://europepmc.org/articles/PMC3591391?pdf=render

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