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

Identification of novel variants in the Cx29 gene of nonsyndromic hearing loss patients using buccal cells and restriction fragment length polymorphism method.

Audiology & neuro-otology - 1 Jan 2010

Wang Wen-Hung, Yang Jiann-Jou, Lin Yen-Chun, Yang Jen-Tsung, Chan Chien-Hui, Li Shuan-Yow

Abstract excerpt

The crucial role of gap junctions, which are composed of connexin (Cx) protein, in auditory functions has been confirmed by numerous studies. Cx29 is a relatively new member of the Cx protein family. In this article, we report variants of the Cx29 gene in 253 unrelated Taiwanese patients with non...

Read the complete abstract on PubMed

Topics

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

Share to Connexins
Share to Cross-Sectional Studies
Share to Deafness

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Genetic Carrier Screening

Share to Nerve Tissue Proteins

Share to Polymorphism, Restriction Fragment Length

Share to Taiwan

Source

Identifiers

PMID: 19657183
DOI: 10.1159/000231633

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19657183-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Identification of novel variants in the Cx29 gene of nonsyndromic hearing loss patients using buccal cells and restriction fragment length polymorphism method.PMID 19657183Read ↗

Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.Semantic proximity Read ↗

Mutations in the connexin 29 gene are not a major cause of nonsyndromic hearing impairment in India.Semantic proximity Read ↗

Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss.Semantic proximity Read ↗

Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss.Semantic proximity Read ↗

Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.Semantic proximity Read ↗

Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness.Semantic proximity Read ↗

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

Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment.Semantic proximity Read ↗

Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss.Semantic proximity Read ↗

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