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Article

FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population.

Gene - 1 Oct 2015

Liu Hong, Gu Zheng, Kang Hou-Yong, Ke Xia, Shen Yang, Wang Xiao-Qiang, Hu Guo-Hua, Zeng Ji-Hong, Hong Su-Ling

Abstract excerpt

Fc receptor-like 3 (FCRL3) has recently been associated with susceptibility to several immune-related diseases. In this study, we evaluated the potential association of FCRL3 polymorphisms with sudden sensorineural hearing loss (SSNHL) in a Chinese Han population. Five single-nucleotide polymorphisms (SNPs) in FCRL3-rs945635, rs3761959, rs7522061, rs10489678, and rs7528684-were genotyped in 630 patients with...

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Source

Identifiers

PMID: 26051414
DOI: 10.1016/j.gene.2015.06.005

Genes

FCRL3
AGT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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