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Article

Alterations in the GJB3 and CLDN14 genes in families with nonsyndromic sensorineural hearing loss.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2005

Arican S T, Incesulu A, Inceoglu B, Tekin M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16259330

Genes

CLDN14
GJB3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Alterations in the GJB3 and CLDN14 genes in families with nonsyndromic sensorineural hearing loss.PMID 16259330Read ↗

The Segregation of p.Arg68Ter-CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene.Semantic proximity Read ↗

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.Semantic proximity Read ↗

Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.Semantic proximity Read ↗

Consensus interpretation of the Met34Thr and Val37Ile variants in <i>GJB2</i> by the ClinGen Hearing Loss Expert PanelSemantic proximity Read ↗

The DFNB1 subtype of autosomal recessive non-syndromic hearing impairment.Semantic proximity Read ↗

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Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.Semantic proximity Read ↗

Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.Semantic proximity Read ↗

Mutation in gap and tight junctions in patients with non-syndromic hearing loss.Semantic proximity Read ↗

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