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

Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.

International journal of pediatric otorhinolaryngology - 1 Sept 2010

Teek Rita, Kruustük Katrin, Zordania Riina, Joost Kairit, Reimand Tiia, Möls Tõnu, Oitmaa Eneli, Kahre Tiina, Tõnisson Neeme, Ounap Katrin

Abstract excerpt

OBJECTIVE: The purpose of this study was to determine the prevalence of c.35delG and p.M34T mutations in the GJB2 gene among children with early onset hearing loss and within a general population of Estonia. METHODS: Using an arrayed primer extension assay, we screened 233 probands with early chi...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Estonia

Share to Europe

Share to Hearing Loss, Sensorineural

Share to Homozygote

Share to Sequence Deletion

Source

Identifiers

PMID: 20708129
DOI: 10.1016/j.ijporl.2010.05.026

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20708129-2026-09-02.2. 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 · 12 closest

Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.PMID 20708129Read ↗

A genotype-phenotype correlation for GJB2 (connexin 26) deafness.Semantic proximity Read ↗

Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness.Semantic proximity Read ↗

Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population.Semantic proximity Read ↗

GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort.Semantic proximity Read ↗

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.Semantic proximity Read ↗

Prevalence of the 35delG mutation in the GJB2 gene in two samples of non-syndromic deaf subjects from Chile.Semantic proximity Read ↗

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

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.Semantic proximity Read ↗

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

Did the GJB2 35delG mutation originate in Iran?Semantic proximity Read ↗

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.Semantic proximity Read ↗

Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population.Semantic proximity Read ↗

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