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Article

Meta-analysis of GJB2 mutation 35delG frequencies in Europe.

Genetic testing - 1 Jan 2001

Lucotte G, Mercier G

Abstract excerpt

Mutations in the gene encoding connexin-26 (specified GJB2) have been shown to be a major cause of nonsyndromic recessive deafness (NSRD), and a single mutation 35delG in the GJB2 gene accounts for the majority of cases of NSRD. This mutation was screened in France and in other European populations by a reliable PCR method. We present here a meta-analysis of the 35delG frequencies in 4123 random controls from 20...

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Source

Identifiers

PMID: 11551104
DOI: 10.1089/109065701753145646

Genes

GJB2

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.

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Meta-analysis of GJB2 mutation 35delG frequencies in Europe.PMID 11551104Read ↗

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