Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.

Acta oto-laryngologica - 1 Aug 2016

Ma Yalin, Xiao Yun, Bai Xiaohui, Zhang Fengguo, Zhang Daogong, Xu Xinmao, Xu Lei, Wang Haibo

Abstract excerpt

CONCLUSION: In this cohort of 156 non-syndromic hearing-impaired subjects of Tengzhou area, the most common deafness-associated genes GJB2, SLC26A4 and mtDNA 12S rRNA were investigated by SNPscan efficiently. GJB2 c.235delC and SLC26A4 c.IVS7-2A > G were the most common mutation sites. OBJECTIVES: Until now, there is no systematic gentic analysis in patients with non-syndromic hearing loss for Tengzhou area, so...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cohort Studies

Share to Connexin 26

Share to Connexins

Share to Deafness

Share to RNA, Ribosomal

Share to Serotonin Plasma Membrane Transport Proteins

Source

Identifiers

PMID: 27066914
DOI: 10.3109/00016489.2016.1164893

Genes

GJB2

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.PMID 27066914Read ↗

Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.Semantic proximity Read ↗

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.Semantic proximity Read ↗

Screening and analysis of mutation hot-spots in deafness-associated genes among adolescents with hearing loss.Semantic proximity Read ↗

Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.Semantic proximity Read ↗

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.Semantic proximity Read ↗

[Analysis of deafness-related gene mutations in 100 non-syndromic hearing loss patients in Henan province].Semantic proximity Read ↗

Establishment of a Gene Detection System for Hotspot Mutations of Hearing Loss.Semantic proximity Read ↗

Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.Semantic proximity Read ↗

[A literature review of epidemiological studies on mutation hot spots of Chinese population with non-syndromic hearing loss].Semantic proximity Read ↗

Application of SNPscan in Genetic Screening for Common Hearing Loss Genes.Semantic proximity Read ↗

[A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss].Semantic proximity Read ↗

[Analysis of common mutations of deafness-related genes in 2725 newborns].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.