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

Human nonsyndromic sensorineural deafness.

Annual review of genomics and human genetics - 1 Jan 2003

Friedman Thomas B, Griffith Andrew J

Abstract excerpt

Given the unique biological requirements of sound transduction and the selective advantage conferred upon a species capable of sensitive sound detection, it is not surprising that up to 1% of the approximately 30,000 or more human genes are necessary for hearing. There are hundreds of monogenic d...

Read the complete abstract on PubMed

Topics

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

Share to Hearing Loss, Sensorineural
Share to Genetic Predisposition to Disease

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14527306
DOI: 10.1146/annurev.genom.4.070802.110347

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14527306-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human nonsyndromic sensorineural deafness.PMID 14527306Read ↗

Mammalian cochlear genes and hereditary deafness.Semantic proximity Read ↗

Hearing loss: a common disorder caused by many rare alleles.Semantic proximity Read ↗

Deafness genes.Semantic proximity Read ↗

Genetics of Hearing and DeafnessSemantic proximity Read ↗

Genes involved in deafness.Semantic proximity Read ↗

Function and expression pattern of nonsyndromic deafness genes.Semantic proximity Read ↗

Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.Semantic proximity Read ↗

Nonsyndromic hearing loss.Semantic proximity Read ↗

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

Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research.Semantic proximity Read ↗

Deafness genes and the mechanism of hearing.Semantic proximity Read ↗

Vestibular and hearing loss in genetic and metabolic disorders.Semantic proximity Read ↗

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