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Article

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

1 Nov 1998

Abstract excerpt

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Topics

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Share to Ear Surgery and Otitis Media
Share to Hearing, Cochlea, Tinnitus, Genetics
Share to Vestibular and auditory disorders

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 9806553
DOI: 10.1038/3118

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionPMID 9806553Read ↗

Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment.Semantic proximity Read ↗

Distinct vestibular phenotypes in DFNA9 families with COCH variants.Semantic proximity Read ↗

Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family.Semantic proximity Read ↗

A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.Semantic proximity Read ↗

Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.Semantic proximity Read ↗

[From gene to disease; a progressive cochlear-vestibular dysfunction with onset in middle-age (DFNA9)].Semantic proximity Read ↗

Auditory phenotype of DFNA1.Semantic proximity Read ↗

Clinical manifestations of DFNB29 deafness.Semantic proximity Read ↗

On the pathophysiology of DFNA9: Effect of pathogenic variants in the COCH gene on inner ear functioning in human and transgenic mice.Semantic proximity Read ↗

Genetic disorders of the vestibular system.Semantic proximity Read ↗

Nonsyndromic hearing impairment is associated with a mutation in DFNA5.Semantic proximity Read ↗

Auditory phenotype of DFNA17.Semantic proximity Read ↗

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