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 regression,...

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Detalles Bibliográficos
Autores principales: Zhao, Shuang-Xia, Liu, Wei, Zhan, Ming, Song, Zhi-Yi, Yang, Shao-Ying, Xue, Li-Qiong, Pan, Chun-Ming, Gu, Zhao-Hui, Liu, Bing-Li, Wang, Hai-Ning, Liang, Liming, Liang, Jun, Zhang, Xiao-Mei, Yuan, Guo-Yue, Li, Chang-Gui, Chen, Ming-Dao, Chen, Jia-Lun, Gao, Guan-Qi, Song, Huai-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591391/
https://www.ncbi.nlm.nih.gov/pubmed/23505439
http://dx.doi.org/10.1371/journal.pone.0057758

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591391/
https://www.ncbi.nlm.nih.gov/pubmed/23505439
http://dx.doi.org/10.1371/journal.pone.0057758

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