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

Article

Phenotypic characterization of hereditary hearing impairment linked to DFNA25.

Archives of otolaryngology--head & neck surgery - 1 Aug 2003

Thirlwall Andrea S, Brown David J, McMillan Pamella M, Barker Susan E, Lesperance Marci M

Abstract excerpt

OBJECTIVES: To clinically characterize a family with nonsyndromic sensorineural hearing loss linked to the DFNA25 gene and to assess whether mitochondrial mutations influence the penetrance of the phenotype. DESIGN: Longitudinal clinical and basic science molecular genetic study. SETTING: Academi...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Audiometry
Share to Disease Progression

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Hearing Loss, Sensorineural

Share to Mitochondria

Share to Surveys and Questionnaires

Share to United States

Source

Identifiers

PMID: 12925340
DOI: 10.1001/archotol.129.8.830

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12925340-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotypic characterization of hereditary hearing impairment linked to DFNA25.PMID 12925340Read ↗

Phenotypic characterization of DFNA24: prelingual progressive sensorineural hearing impairment.Semantic proximity Read ↗

Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.Semantic proximity Read ↗

Audiological follow-up of children with the m.1555A>G mutation in mitochondrial DNA.Semantic proximity Read ↗

New insights into the complex genetic architecture of age-related hearing loss.Semantic proximity Read ↗

Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37.Semantic proximity Read ↗

Hereditary deafness and phenotyping in humans.Semantic proximity Read ↗

A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13.Semantic proximity Read ↗

Clinical manifestations of DFNB29 deafness.Semantic proximity Read ↗

Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study.Semantic proximity Read ↗

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

The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.Semantic proximity Read ↗

Distinctive audiometric profile associated with DFNB21 alleles of <i>TECTA</i>Semantic proximity Read ↗

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