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

Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation.

The Laryngoscope - 1 Feb 2002

Tamagawa Yuya, Ishikawa Kazuhiro, Ishikawa Kotaro, Ishida Takashi, Kitamura Ken, Makino Shinji, Tsuru Tadahiko, Ichimura Keiichi

Abstract excerpt

OBJECTIVES/HYPOTHESIS: To characterize the audiovestibular phenotype of DFNA11, an autosomal dominant nonsyndromic hearing impairment caused by a mutation in the myosin VIIA gene (MYO7A), including whether DFNA11-affected subjects have retinal degeneration as is characteristic of Usher syndrome type 1B, caused by different MYO7A mutations. STUDY DESIGN: Retrospective study of audiovestibular and ophthalmological...

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 Audiometry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dyneins

Share to Formins

Share to Hearing Loss, Sensorineural

Share to Incidence

Share to Myosin VIIa

Share to Myosins

Source

Identifiers

PMID: 11889386
DOI: 10.1097/00005537-200202000-00017

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

Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation.PMID 11889386Read ↗

The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B.Semantic proximity Read ↗

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11.Semantic proximity Read ↗

In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.Semantic proximity Read ↗

Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11).Semantic proximity Read ↗

[From gene to disease; DFNA8/12, an autosomal dominant inherited bowl-shaped sensorineural hearing impairment].Semantic proximity Read ↗

Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant MYO7A-Associated Hearing Loss Patients.Semantic proximity Read ↗

The Clinical Details of MYH9-Related Disease and DFNA17 in a Large Japanese Hearing Loss Cohort.Semantic proximity Read ↗

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

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.Semantic proximity Read ↗

Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).Semantic proximity Read ↗

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.Semantic proximity Read ↗

A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder.Semantic proximity Read ↗

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