Auditory phenotype of DFNA1.

doi:10.1159/000066801

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Auditory phenotype of DFNA1.

Advances in oto-rhino-laryngology - 1 Jan 2002

Leon Pedro E, Lalwani Anil K

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adaptor Proteins, Signal Transducing
Share to Age of Onset
Share to Carrier Proteins
Share to Child

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

Share to Deafness

Share to Disease Progression

Share to Formins

Share to Pedigree

Source

Open in PubMed

Identifiers

PMID: 12408060
DOI: 10.1159/000066801

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

Auditory phenotype of DFNA1.PMID 12408060Read ↗

Auditory phenotype of DFNA17.Semantic proximity Read ↗

DFNA9/COCH and its phenotype.Semantic proximity Read ↗

Histopathology of the inner ear in DFNA9.Semantic proximity Read ↗

Clinical manifestations of DFNB29 deafness.Semantic proximity Read ↗

Non-syndromic dominant DFNA1.Semantic proximity Read ↗

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

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

Using genetics to understand auditory function and improve diagnosis.Semantic proximity Read ↗

Sensorineural hearing impairment: non-syndromic, recessive DFNB2.Semantic proximity Read ↗

Hearing impairment: a panoply of genes and functions.Semantic proximity Read ↗

Mutations in COCH (formerly Coch5b2) cause DFNA9.Semantic proximity Read ↗

Genetic causes of hearing loss.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.