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

Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss.

Medicine - 1 Jun 2017

Han Rui, Li Linge, Duan Ling, Xia Yan, Kuyaxi Pilidong, Zhao Juan, Zhao Qi, Zhang Hua, Chen Yu

Abstract excerpt

We aim to screen the mutations of 3 hearing loss (HL) genes (GJB2, SLC26A4, and 12S rRNA) in 71 cases with nonsyndromic hearing loss (NSHL) using microarray and SNPscan, and identify the roles of nonhotspot mutation of these genes in the screening of NSHL. Seventy-one cases with moderate or severe neurosensory deafness confirmed in our department from July 2014 to December 2015 including 25 Uyghur minorities and...

Read the complete abstract on PubMed

Topics

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

Share to Connexin 26
Share to Connexins
Share to Deafness

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Membrane Transport Proteins

Share to Microarray Analysis

Share to RNA, Ribosomal

Share to Sulfate Transporters

Source

Open in PubMed Open full text

Identifiers

PMID: 28640090
DOI: 10.1097/MD.0000000000007149
PMCID: PMC5484198

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss.PMID 28640090Read ↗

Application of SNPscan in Genetic Screening for Common Hearing Loss Genes.Semantic proximity Read ↗

Microarray-based mutation detection of pediatric sporadic nonsyndromic hearing loss in China.Semantic proximity Read ↗

Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.Semantic proximity Read ↗

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss.Semantic proximity Read ↗

Detection of hereditary hearing loss gene by DNA microarray.Semantic proximity Read ↗

SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.Semantic proximity Read ↗

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.Semantic proximity Read ↗

GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.Semantic proximity Read ↗

Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.Semantic proximity Read ↗

An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population.Semantic proximity Read ↗

Application of gene detection technique in the antenatal diagnosis of hereditary hearing loss.Semantic proximity Read ↗

[A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss].Semantic proximity Read ↗

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