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

Connexin26 gene ( GJB2): prevalence of mutations in the Chinese population.

Journal of human genetics - 1 Jan 2002

Liu Yuhe, Ke Xiaomei, Qi Yu, Li Wei, Zhu Ping

Abstract excerpt

The connexin26 gene ( GJB2) has been shown to be responsible for DFNB1 and DFNA3 (Autosomal Recessive Hereditary Nonsyndromic Deafness Locus 1 and Autosomal Dominant Hereditary Nonsyndromic Deafness Locus 3). Two hundred ten independently ascertained Chinese probands with nonsyndromic hearing loss (NSHL) were evaluated for mutations in GJB2, including 43 probands from families with more than one sib with NSHL,...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Asian People
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexin 26

Share to Connexins

Share to Gene Frequency

Share to Genetic Predisposition to Disease

Share to Hearing Loss

Source

Identifiers

PMID: 12522692
DOI: 10.1007/s100380200106

Genes

GJB2

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

Connexin26 gene ( GJB2): prevalence of mutations in the Chinese population.PMID 12522692Read ↗

The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.Semantic proximity Read ↗

Prevalent connexin 26 gene (GJB2) mutations in Japanese.Semantic proximity Read ↗

High prevalence of the connexin 26 (GJB2) mutation in Chinese cochlear implant recipients.Semantic proximity Read ↗

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.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 ↗

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.Semantic proximity Read ↗

Connexin26 mutations associated with nonsyndromic hearing loss.Semantic proximity Read ↗

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.Semantic proximity Read ↗

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.Semantic proximity Read ↗

Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese family.Semantic proximity Read ↗

A novel connexin 26 compound heterozygous mutation results in deafness.Semantic proximity Read ↗

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.Semantic proximity Read ↗

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