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

[Study of a mutation in connexin 26 gene associated with congenital sensorineural deafness].

Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology - 1 Oct 2001

Wang P, Wang Y, Liu X, Du B

Abstract excerpt

OBJECTIVE: So far, at least 39 deafness gene loci have been mapped in human chromosome including the connexin 26 gene coding for a gap-junction protein. This gene is thought to be linked to hereditary non-syndromic sensorineural hearing loss. About 80% of cases of DFNB1 hereditary deafness carry a 30 mer G mutation of connexin 26. METHOD: To investigate this relationship, we obtained DNA samples from 15 cases...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Connexin 26

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to Hearing Loss, Sensorineural

Share to Mutation

Source

Identifiers

PMID: 12541685

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Study of a mutation in connexin 26 gene associated with congenital sensorineural deafness].PMID 12541685Read ↗

[Mutations in the connexin 26 gene in patients with nonsyndromic hearing impairment].Semantic proximity Read ↗

[Study on mutations in the connexin 26 gene among Chinese with nonsyndromic hearing loss].Semantic proximity Read ↗

[Mutation analysis of Cx26 gene in Chinese hereditary nonsyndromic deafness sufferers].Semantic proximity Read ↗

[From gene to disease: deafness and connexin 26].Semantic proximity Read ↗

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.Semantic proximity Read ↗

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

[Application of next generation sequencing in congenital sensorineural deafness].Semantic proximity Read ↗

A novel compound heterozygous mutation (35delG, 363delC) in the Connexin 26 gene causes non-syndromic autosomal recessive hearing loss.Semantic proximity Read ↗

[Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].Semantic proximity Read ↗

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

Advances in hereditary deafness.Semantic proximity Read ↗

[Genetic deafness:the primary cause of sensorineural hearing loss in children].Semantic proximity Read ↗

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