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

Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.

International journal of pediatric otorhinolaryngology - 1 May 2018

Huang Bangqing, Han Mingyu, Wang Guojian, Huang ShaSha, Zeng Jialing, Yuan Yongyi, Dai Pu

Abstract excerpt

OBJECTIVES: To provide appropriate genetic testing and counseling for non-syndromic hearing impairment patients in Hainan Province, an island in the South China Sea. METHODS: 299 unrelated students with non-syndromic hearing loss who attended a special education school in Hainan Province were enrolled in this study. Three prominent deafness-related genes (GJB2, SLC26A4, and mtDNA 12S rRNA) were analyzed using...

Read the complete abstract on PubMed

Topics

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

Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deafness

Share to DNA, Mitochondrial

Share to High-Throughput Nucleotide Sequencing

Share to Membrane Transport Proteins

Share to RNA, Ribosomal

Share to Sulfate Transporters

Source

Identifiers

PMID: 29605365
DOI: 10.1016/j.ijporl.2018.02.015

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

Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.PMID 29605365Read ↗

Gene Screening for Non-Syndromic Deafness in Hainanese Patients.Semantic proximity Read ↗

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

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

Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study.Semantic proximity Read ↗

Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China.Semantic proximity Read ↗

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.Semantic proximity Read ↗

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

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

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

Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.Semantic proximity Read ↗

Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss.Semantic proximity Read ↗

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