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 carrier frequency of the GJB2 mutation (35delG) in the north of Iran.

International journal of pediatric otorhinolaryngology - 1 Jun 2007

Chaleshtori Morteza Hashemzadeh, Farrokhi Effat, Shahrani Mehrdad, Kheiri Soleiman, Dolati Masoumeh, Rad Laleh Hoghooghi, Pour-Jafari Hamid, Samani Keihan Ghatreh, Chaleshtori Katayoon Safa, Crosby Andrew H

Abstract excerpt

OBJECTIVE: Mutations in the GJB2 gene are a major cause of autosomal recessive and sporadic non-syndromic hearing loss in many populations. A single mutation of this gene (35delG) accounts for approximately 70% of mutations in Caucasians with a carrier frequency of 2-4% in Europe. This study aims...

Read the complete abstract on PubMed

Topics

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

Share to Base Pairing
Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrophoresis

Share to Genetic Carrier Screening

Share to Guanine

Share to Hearing Loss

Share to Middle East

Source

Identifiers

PMID: 17428550
DOI: 10.1016/j.ijporl.2007.02.005

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17428550-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

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

High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.PMID 17428550Read ↗

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

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.Semantic proximity Read ↗

Determination of the carrier frequencies of selected GJB2 mutations in the Korean population.Semantic proximity Read ↗

Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran.Semantic proximity Read ↗

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

A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.Semantic proximity Read ↗

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

GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran.Semantic proximity Read ↗

Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.Semantic proximity Read ↗

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.Semantic proximity Read ↗

High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness.Semantic proximity Read ↗

Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions.Semantic proximity Read ↗

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