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Association Between Susceptibility to SSHL and Single Nucleotide Polymorphisms at the rs2228612 Locus of the DNMT1 Gene and the rs5570459 Locus of the GJB2 Gene.

Alternative therapies in health and medicine - 1 Apr 2023

Zhang Yanyan, Liu Hua, Song Yang, Liu Ning, Yao Cunjun

Abstract excerpt

Context: Sudden deafness (SSHL) belongs to the category of diseases causing neurological hearing loss with a sudden and unknown etiology. The pathogenesis and mechanism of SSHL aren't clear at present. Gene polymorphisms may be associated with increased or reduced risk of hearing impairment. Objective: The study intended to investigate the association between susceptibility to SSHL and single nucleotide...

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PMID: 36795524

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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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