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

Nonsyndromic X-linked hearing loss.

Frontiers in bioscience (Elite edition) - 1 Jan 2012

Song Mee Hyun, Lee Kyu-Yup, Choi Jae Young, Bok Jinwoong, Kim Un-Kyung

Abstract excerpt

To date, 135 loci and 50 genes have been identified as causes of nonsyndromic hearing loss. Until recently, four loci (DFN2, DFN3, DFN4, and DFN6) had been implicated in nonsyndromic X-linked hearing loss; however, a new classification (DFNX1-5) has been proposed to reduce confusion in the terminology. The different types of nonsyndromic X-linked hearing loss demonstrate various clinical features in terms of the...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Diseases, X-Linked
Share to Genetic Predisposition to Disease
Share to Hearing Loss

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Source

Identifiers

PMID: 22201925
DOI: 10.2741/E430

Genes

PRPS1

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nonsyndromic X-linked hearing loss.PMID 22201925Read ↗

De Novo Mutation in X-Linked Hearing Loss–Associated POU3F4 in a Sporadic Case of Congenital Hearing LossSemantic proximity Read ↗

X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.Semantic proximity Read ↗

Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population.Semantic proximity Read ↗

[Non-syndromic hereditary hearing impairment].Semantic proximity Read ↗

A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss.Semantic proximity Read ↗

Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2.Semantic proximity Read ↗

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.Semantic proximity Read ↗

Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.Semantic proximity Read ↗

Nonsyndromic hereditary hearing loss.Semantic proximity Read ↗

Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.Semantic proximity Read ↗

<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing lossSemantic proximity Read ↗

Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome.Semantic proximity Read ↗

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