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

[The roles of connexin genes in sporadic hearing loss population].

Zhonghua yi xue za zhi - 24 Apr 2007

Li Qing-zhong, Wang Qiu-ju, Chi Fang-lu, Li Li-na, Zhao Ya-li, Yuan Hu, Han Dong-yi

Abstract excerpt

OBJECTIVE: To investigate the roles of connexin genes in Chinese population. METHODS: Peripheral blood samples were collected from 214 patients with hearing loss, 160 with sensorineural hearing loss (66 with prelingual hearing loss and 94 with postlingual hearing loss), 32 with auditory neuropathy, and 22 with enlarged vestibular aqueduct syndrome (EVAS), 110 males and 104 females, all from 14 provinces north of...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Connexin 26
Share to Connexin 30

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to Gene Frequency

Share to Genetic Variation

Share to Hearing Loss

Share to Mutation

Source

Identifiers

PMID: 17672988

Genes

GJB6
GJB2
GJB3

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

[The roles of connexin genes in sporadic hearing loss population].PMID 17672988Read ↗

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

Update of the spectrum of GJB2 mutations in 107 patients with nonsyndromic hearing loss in the Fujian population of China.Semantic proximity Read ↗

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

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

[A hereditary hearing loss case accompanied by unilateral sudden hearingloss:GJB2 235delC homozygotes related late-onsetmoderate hearing impairment].Semantic proximity Read ↗

[Mutation analysis of GJB2 gene in 1 822 patients with nonsyndromic hearing loss in Zhejiang Province].Semantic proximity Read ↗

GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss.Semantic proximity Read ↗

[Genotype and clinical phenotype analysis of 42 patients with delayed nonsyndromic hearing loss].Semantic proximity Read ↗

[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].Semantic proximity Read ↗

Efficacy of Connexin testing in detecting Non-syndromic Sensorineural Hearing Loss in an Indian cohortSemantic proximity Read ↗

[Analysis of GJB2 gene and mitochondrial DNA A1555G mutations in 16 families with non-syndromic hearing loss].Semantic proximity Read ↗

[Analysis of genotype-phenotype correlation for GJB2 in 221 non-syndromic deafness probands and their pedigrees].Semantic proximity Read ↗

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