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

Molecular screening of patients with profound hearing loss from Chengdu, China.

Acta oto-laryngologica - 1 Jan 2022

Dai Qingqing, Dai Wei, Wang Dan, Liu Xia, Zou Ling, Chen Jiani, Zheng Hong, Duan Maoli

Abstract excerpt

BACKGROUND: The rate of genetic deafness in Chengdu is still underestimated. OBJECTIVE: To investigate patients' molecular etiology with profound hearing loss and facilitate genetic counseling for their families, we screened deafness-related genes of profound hearing loss in the population. METHODS: A total of 1427 unrelated patients with profound hearing loss containing all age groups in the administrative area...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Connexin 26
Share to DNA Mutational Analysis

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

Share to Genes, Mitochondrial

Share to Genomics

Share to Hearing Loss

Share to Infant

Share to Sulfate Transporters

Source

Identifiers

PMID: 34936523
DOI: 10.1080/00016489.2021.2014564

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

Molecular screening of patients with profound hearing loss from Chengdu, China.PMID 34936523Read ↗

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

Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern 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 ↗

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

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.Semantic proximity Read ↗

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.Semantic proximity Read ↗

[Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].Semantic proximity Read ↗

Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.Semantic proximity Read ↗

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.Semantic proximity Read ↗

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.Semantic proximity Read ↗

[Analysis of common mutations of deafness-related genes in 2725 newborns].Semantic proximity Read ↗

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

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