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Article

Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes.

Human molecular genetics - 15 May 2012

McKinney Cushla, Merriman Tony R

Abstract excerpt

Although deletion in the low-affinity IgG receptor gene FCGR3B has repeatedly been implicated in systemic autoimmune disease, the role of FCGR3B copy number variation (CNV) in autoimmunity still remains unclear. Factors such as study size, ethnicity, specific disease phenotype and experimental methodology may explain these conflicting results. Here we aimed at using meta-analysis to assess the role for FCGR3B CNV...

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Share to Autoimmune Diseases
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22337955
DOI: 10.1093/hmg/dds039

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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