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

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

Acta oto-laryngologica - 1 Mar 2008

Guo Yu-Fen, Liu Xiao-Wen, Guan Jing, Han Ming-Kun, Wang Da-Yong, Zhao Ya-Li, Rao Shao-Qi, Wang Qiu-Ju

Abstract excerpt

CONCLUSION: This genetic epidemiological study demonstrated that 26.65% of the prelingual deafness in Northern Chinese patients can be detected at younger ages by genetic testing of three common hearing loss genes (GJB2, SLC26A4 and mtDNA A1555G), and thus, early intervention measures could be undertaken to help them in language acquisition. OBJECTIVES: The GJB2, SLC26A4 and mtDNA A1555G mutations are the...

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 Delete account & data About Contact Helena Bioinformatics

Share to DNA, Mitochondrial

Share to Genetic Carrier Screening

Share to Genetic Testing

Share to Homozygote

Share to Reference Values

Source

Identifiers

PMID: 18274916
DOI: 10.1080/00016480701767382

Genes

GJB2

Variants

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

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.PMID 18274916Read ↗

Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.Semantic proximity Read ↗

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.Semantic proximity Read ↗

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

GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.Semantic proximity Read ↗

Comparison of the Mutation Spectrum of Common Deafness-Causing Genes in 509 Patients With Nonsyndromic Hearing Loss in 4 Different Areas of China by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry.Semantic proximity Read ↗

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

GJB2 and mitochondrial DNA 1555A>G mutations in students with hearing loss in the Hubei Province of China.Semantic proximity Read ↗

Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.Semantic proximity Read ↗

The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide.Semantic proximity Read ↗

Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants.Semantic proximity Read ↗

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

Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum.Semantic proximity Read ↗

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