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Article

The c.IVS1+1G>A mutation in the GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population.

Journal of genetics - 1 Dec 2006

Sirmaci Asli, Akcayoz-Duman Duygu, Tekin Mustafa

Abstract excerpt

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Topics

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Share to Genetic Testing
Share to Connexin 26
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Share to Electrophoresis, Agar Gel

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Deletion

Share to Hearing Loss, Sensorineural

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Source

Identifiers

PMID: 17406097
DOI: 10.1007/BF02935334

Genes

GJB2
GJB6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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The c.IVS1+1G>A mutation in the GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population.PMID 17406097Read ↗

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

Wan Du et al. - Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants. Acta Oto-Laryngol 2014; 134: 373-381.Semantic proximity Read ↗

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Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants.Semantic proximity Read ↗

KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr).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 ↗

GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment.Semantic proximity Read ↗

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GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.Semantic proximity Read ↗

First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.Semantic proximity Read ↗

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GJB2 and mitochondrial DNA 1555A>G mutations in students with hearing loss in the Hubei Province of China.Semantic proximity Read ↗

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