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

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology - 1 Sept 2004

Makishima Tomoko, Kurima Kiyoto, Brewer Carmen C, Griffith Andrew J

Abstract excerpt

OBJECTIVE: To characterize the auditory and vestibular phenotype of autosomal dominant nonsyndromic DFNA36 hearing loss. STUDY DESIGN: Clinical evaluation of individuals with DFNA36 hearing loss linked to the D572N mutation of transmembrane channel-like gene 1 (TMC1). Medical history interviews, physical examinations, and pure-tone air conduction audiometry were performed in the field. Audiology and radiology...

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, Pure-Tone

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Auditory Threshold

Share to Cross-Sectional Studies

Share to Disease Progression

Share to Hearing Loss, Sensorineural

Share to Pedigree

Share to Regression Analysis

Source

Identifiers

PMID: 15354000
DOI: 10.1097/00129492-200409000-00011

Genes

TMC1

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.PMID 15354000Read ↗

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

Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis.Semantic proximity Read ↗

Gradual Symmetric Progression of DFNA34 Hearing Loss Caused by an NLRP3 Mutation and Cochlear Autoinflammation.Semantic proximity Read ↗

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

KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.Semantic proximity Read ↗

The DFNA10 phenotype.Semantic proximity Read ↗

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

Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss.Semantic proximity Read ↗

Phenotypic characterization of hereditary hearing impairment linked to DFNA25.Semantic proximity Read ↗

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.Semantic proximity Read ↗

Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1.Semantic proximity Read ↗

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