Discover Community Create You

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

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

Clinical otolaryngology and allied sciences - 1 Aug 2001

Ensink R J, Huygen P L, Snoeckx R L, Caethoven G, Van Camp G, Cremers C W

Abstract excerpt

We present a Dutch family with autosomal dominantly inherited mid-frequency and high-frequency sensorineural hearing impairment. Genetic linkage analysis in this family indicated linkage to DFNA13 with logarithm of the odds ratio (LOD) scores > +4. The majority of the affected persons presented with hearing impairment from the age of 30 years onwards, although hearing impairment was noted at about 10 years of age...

Read the complete abstract on PubMed

Topics

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

Share to Audiometry, Pure-Tone
Share to Cross-Sectional Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Disease Progression

Share to Family

Share to Genes, Dominant

Share to Genetic Linkage

Share to Hearing Loss, Sensorineural

Share to Netherlands

Source

Identifiers

PMID: 11559344
DOI: 10.1046/j.1365-2273.2001.00477.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13.PMID 11559344Read ↗

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

A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region.Semantic proximity Read ↗

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.Semantic proximity Read ↗

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

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

Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p.Semantic proximity Read ↗

Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1-2q23.3.Semantic proximity Read ↗

Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).Semantic proximity Read ↗

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.Semantic proximity Read ↗

Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.Semantic proximity Read ↗

[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].Semantic proximity Read ↗

Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment.Semantic proximity Read ↗

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