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

High frequency of heterozygosity in GJB2 mutations among patients with non-syndromic hearing loss.

The Journal of laryngology and otology - 1 Mar 2009

Khandelwal G, Bhalla S, Khullar M, Panda N K

Abstract excerpt

OBJECTIVE: To determine the prevalence of GJB2 mutations among subjects with congenital, non-syndromic, sensorineural hearing loss, within a north Indian population. MATERIALS AND METHODS: This was a case-control study in which the frequencies of the three most prevalent GJB2 mutations (35delG, W24X and 167delT) were studied. Polymerase chain reaction restriction fragment length polymorphism assays were performed...

Read the complete abstract on PubMed

Topics

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

Share to Codon, Nonsense
Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Hearing Loss, Sensorineural

Share to Heterozygote

Share to Infant

Source

Identifiers

PMID: 18570691
DOI: 10.1017/S0022215108002892

Genes

GJB2

Variants

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

High frequency of heterozygosity in GJB2 mutations among patients with non-syndromic hearing loss.PMID 18570691Read ↗

Frequency of GJB2 mutations in patients with nonsyndromic hearing loss from an ethnically characterized Brazilian population.Semantic proximity Read ↗

Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario.Semantic proximity Read ↗

Low frequency of GJB2 mutations in thirty-five students with hearing loss in Chinese consanguineous families.Semantic proximity Read ↗

High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.Semantic proximity Read ↗

GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment.Semantic proximity Read ↗

High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India.Semantic proximity Read ↗

Incidence of the 35delG/GJB2 mutation in low-risk newborns.Semantic proximity Read ↗

Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment.Semantic proximity Read ↗

GJB2 mutations: Genotypic and phenotypic correlation in a cohort of 690 hearing-impaired patients, toward a new mutation?Semantic proximity Read ↗

Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss.Semantic proximity Read ↗

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.Semantic proximity Read ↗

Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment.Semantic proximity Read ↗

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