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

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

BioMed research international - 1 Jan 2016

Zhang Fengguo, Xiao Yun, Xu Lei, Zhang Xue, Zhang Guodong, Li Jianfeng, Lv Huaiqing, Bai Xiaohui, Wang Haibo

Abstract excerpt

Hearing loss is a common sensory disorder, and at least 50% of cases are due to a genetic etiology. Although hundreds of genes have been reported to be associated with nonsyndromic hearing loss, GJB2, SLC26A4, and mtDNA12SrRNA are the major contributors. However, the mutation spectrum of these common deafness genes varies among different ethnic groups. The present work summarized mutations in these three genes...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Connexin 26

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to DNA Mutational Analysis

Share to Hearing Loss

Share to Infant

Share to Membrane Transport Proteins

Share to Sulfate Transporters

Source

Open in PubMed Open full text

Identifiers

PMID: 27247933
DOI: 10.1155/2016/1302914
PMCID: PMC4876198

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

Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.PMID 27247933Read ↗

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss.Semantic proximity Read ↗

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

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

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

Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.Semantic proximity Read ↗

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

[Detection of common deafness-related genes among non-syndromic deafness patients from Shanxi province].Semantic proximity Read ↗

Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss.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 ↗

[A new method for simultaneous multi-gene mutation screening in 355 patients with nonsyndromic hearing loss of Inner Mongolia Autonomous region].Semantic proximity Read ↗

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