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 GJB2, GJB3 and GJB6 gene in deaf population from special educational school of Chifeng city].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 Jan 2008

Yuan Yongyi, Huang Deliang, Dai Pu, Zhu Xiuhui, Yu Fei, Zhang Xin, Liu Lixian, Han Dongyi

Abstract excerpt

OBJECTIVE: To investigate the genetic causes of nonsyndromic deaf patients in special educational school of Chifeng city. Inner Mongolia by genetic screening testing method. This study focused on analyzing mutations of coding sequence of GJB2, GJB3 and GJB6 gene. METHOD: DNA were extracted out from peripheral blood of 134 nonsyndromic deaf probands of Chifeng special educational school and 100 normal hearing...

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 Connexin 26

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexin 30

Share to Connexins

Share to Genetic Testing

Share to Hearing Loss

Share to Heterozygote

Share to Students

Source

Identifiers

PMID: 18338563

Genes

GJB2
GJB3
GJB6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mutation analysis of GJB2, GJB3 and GJB6 gene in deaf population from special educational school of Chifeng city].PMID 18338563Read ↗

[Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].Semantic proximity Read ↗

[Sequence analysis of GJB3 in Chinese deafness population who carry one heterozygous GJB2 pathogenic mutation].Semantic proximity Read ↗

[GJB6 gene mutation analysis in Chinese nonsyndromic deaf population].Semantic proximity Read ↗

[The sequencing analyze of 915 newborn with GJB2 heterozygous mutation in Beijing].Semantic proximity Read ↗

[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases].Semantic proximity Read ↗

[Sequencing of 100 common variation sites of 18 deafness susceptibility genes among 16 182 individuals from Dongguan].Semantic proximity Read ↗

[Analysis of deafness-related gene mutations in 23 nonsyndromic hearing impairment families in Guangxi Zhuang Autonomous Region].Semantic proximity Read ↗

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

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.Semantic proximity Read ↗

[An analysis of the mutation in GJB2，GJB3，SLC26A4 and mtDNA12SrRNA in new born].Semantic proximity Read ↗

Prevalence of GJB6 mutations in Chinese patients with non-syndromic hearing loss.Semantic proximity Read ↗

GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness.Semantic proximity Read ↗

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