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Article

Connexin 26 mutation 35delG: prevalence of carriers in various regions in France.

International journal of pediatric otorhinolaryngology - 1 Sept 2005

Mercier Géraldine, Bathelier Christian, 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 1/30 in Mediterranean countries. The aim of this study is to determinate the percentage of carriers in several regions of the Mediterranean coast in France. METHODS: This study has been carried out on the genomic DNAs out of a total of 1584...

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Identifiers

PMID: 15878206
DOI: 10.1016/j.ijporl.2005.03.009

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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.

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