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Article

Association study of copy number variants in FCGR3A and FCGR3B gene with risk of ankylosing spondylitis in a Chinese population.

Rheumatology international - 1 Mar 2016

Wang Li, Yang Xiao, Cai Guoqi, Xin Lihong, Xia Qing, Zhang Xu, Li Xiaona, Wang Mengmeng, Wang Kang, Xia Guo, Xu Shengqian, Xu Jianhua, Zou Yanfeng, Pan Faming

Abstract excerpt

Ankylosing spondylitis (AS) is a common inherited autoimmune disease. Copy number variation (CNV) of DNA segments has been found to be an important part of genetic variation, and the FCGR3A and FCGR3B gene CNVs have been associated with various autoimmune disorders. The aim of the study was to determine whether CNVs of FCGR3A and FCGR3B were also associated with the susceptibility of AS. A total of 801...

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PMID: 26494566
DOI: 10.1007/s00296-015-3384-0

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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