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

[Mutation analysis of Cx26 gene in Chinese hereditary nonsyndromic deafness sufferers].

Zhonghua er bi yan hou ke za zhi - 1 Oct 2002

Xu Yuefan, Ren Lufeng, Song Wenqin, Zhang Changjun, Ma Yuanxu, Li Jinchun, Zhang Yanni

Abstract excerpt

OBJECTIVE: To analyze the mutations in the code region of Cx26 gene in Chinese hereditary nonsyndromic hearing impairment (NSHI) sufferers. METHODS: Thirty-three cases (29 cases in the families of 8 students who were picked out from the Deafness and Muteness School of Tianjin, 2 cases as control and 2 normal cases of genetic counseling) were included in this study. The blood samples were obtained to distill the...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Child
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexin 26

Share to Connexins

Share to DNA Mutational Analysis

Share to Hearing Loss, Sensorineural

Share to Pedigree

Source

Identifiers

PMID: 12772454

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

[Mutation analysis of Cx26 gene in Chinese hereditary nonsyndromic deafness sufferers].PMID 12772454Read ↗

[Mutations in the connexin 26 gene in patients with nonsyndromic hearing impairment].Semantic proximity Read ↗

[Study on mutations in the connexin 26 gene among Chinese with nonsyndromic hearing loss].Semantic proximity Read ↗

[Study of a mutation in connexin 26 gene associated with congenital sensorineural deafness].Semantic proximity Read ↗

[Sequence analysis of the connexin 26 genes from a deafness family with A1555G mutation in Huaiyin].Semantic proximity Read ↗

A novel compound heterozygous mutation (35delG, 363delC) in the Connexin 26 gene causes non-syndromic autosomal recessive hearing loss.Semantic proximity Read ↗

Connexin26 mutations associated with nonsyndromic hearing loss.Semantic proximity Read ↗

[Analysis of deafness-related gene mutations in 23 nonsyndromic hearing impairment families in Guangxi Zhuang Autonomous Region].Semantic proximity Read ↗

[GJB6 gene mutation analysis in Chinese nonsyndromic deaf population].Semantic proximity Read ↗

[Mutations of Cx26 gene in patients with NSHL and intracellular distribution of two mutants].Semantic proximity Read ↗

[SLC26A4 mutations in a Chinese deafness family discovered by next-generation sequencing technology].Semantic proximity Read ↗

Molecular analysis of SLC26A4 gene in a Chinese deafness family.Semantic proximity Read ↗

[Practical medico-genetic counseling for congenital and early loss of hearing in children].Semantic proximity Read ↗

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