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 prevalences of carriers of the 35delG mutation of connexin 26 in the Mediterranean area.

International journal of pediatric otorhinolaryngology - 1 May 2007

Lucotte Gérard

Abstract excerpt

OBJECTIVE: Mutation 35delG in the connexin 26 gene is the main cause of recessive deafness in Europe. The prevalence of carriers varies, with a mean value proportion of 1/31 in Mediterranean countries. The aim of this study is to determinate the percentage of carriers in seven populations of the Mediterranean area and to compare prevalence of the mutation in seventeen other published populations in the same area....

Read the complete abstract on PubMed

Topics

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

Share to Connexin 26
Share to Connexins
Share to Deafness

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Carrier Screening

Share to Genomics

Share to Mediterranean Region

Share to Point Mutation

Share to Prevalence

Source

Identifiers

PMID: 17316834
DOI: 10.1016/j.ijporl.2007.01.010

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

High prevalences of carriers of the 35delG mutation of connexin 26 in the Mediterranean area.PMID 17316834Read ↗

Connexin 26 mutation 35delG: prevalence of carriers in various regions in France.Semantic proximity Read ↗

The 35delG mutation in the connexin 26 gene (GJB2) associated with congenital deafness: European carrier frequencies and evidence for its origin in ancient Greece.Semantic proximity Read ↗

Frequencies of two common mutations (c.35delG and c.167delT) of the connexin 26 gene in different populations of Hungary.Semantic proximity Read ↗

Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.Semantic proximity Read ↗

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.Semantic proximity Read ↗

Connexin 26 (GJB2) Gene Mutations Linked With Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in Iraqi Population.Semantic proximity Read ↗

Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.Semantic proximity Read ↗

Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness.Semantic proximity Read ↗

Frequency of the 35delG allele causing nonsyndromic recessive deafness in the Algerian patients.Semantic proximity Read ↗

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

[The mutation 35delG of the gene of the connexin 26 is a frequent cause of autosomal-recessive non-syndromic hearing loss in Morocco].Semantic proximity Read ↗

Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey.Semantic proximity Read ↗

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