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Article

Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients.

Clinical genetics - 1 Dec 2001

Bariş I, Kilinç M O, Tolun A

Abstract excerpt

The 35delG mutation in the connexin 26 gene (GJB2) at the DFNB1 locus is the most common mutation in patients with autosomal-recessive sensorineural deafness. Genetic diagnosis is crucial for genetic counseling. We have developed an easy and simple method and screened a total of 235 unrelated hearing-impaired children. We found 48 of the subjects to be homozygous for the mutation, including 27 of 83 familial...

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Source

Identifiers

PMID: 11846738
DOI: 10.1034/j.1399-0004.2001.600608.x

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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