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

[Analysis on GJB2 gene mutations with nonsyndromic hearing impairment in Kazak patients of Xinjiang].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 May 2014

Wang Changwei, Cai Xiaoniu, Zou Guanghua, Tie Ling, Li Yanhua

Abstract excerpt

OBJECTIVE: To study mutations in the GJB2 gene in Kazak patients with nonsyndromic hearing impairment from Xinjiang. METHOD: One hundred and ninety-three cases of Kazak from the Xinjiang region, including 97 cases of hearing loss and 96 cases of normal people, were performed mutational analysis of the GJB2 coding region by PCR-direct sequencing. RESULT: Eight kinds of mutation were found in the encoding region of...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexin 26

Share to Connexins

Share to Deafness

Share to Ethnicity

Share to Infant

Share to Young Adult

Source

Identifiers

PMID: 25129963

Genes

GJB2

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis on GJB2 gene mutations with nonsyndromic hearing impairment in Kazak patients of Xinjiang].PMID 25129963Read ↗

[Study on nonsyndromic hereditary hearing impairment mutations of GJB2 gene in Uyghur patients in Xinjiang].Semantic proximity Read ↗

[Mutation analysis of GJB2 gene in 1 822 patients with nonsyndromic hearing loss in Zhejiang Province].Semantic proximity Read ↗

[Epidemiological analysis of GJB2,SLC26A4,mtRNA,GJB3 in nonsyndromic hearing loss in Kashi in Xinjiang].Semantic proximity Read ↗

[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases].Semantic proximity Read ↗

[Common gene mutations study in Uyghur population with deafness in Kashgar region of Xinjiang].Semantic proximity Read ↗

[Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang].Semantic proximity Read ↗

[Prevalence of GJB2 mutations in Uigur and Han ethnic populations with deafness in Xinjiang region of China].Semantic proximity Read ↗

Update of the spectrum of GJB2 mutations in 107 patients with nonsyndromic hearing loss in the Fujian population of China.Semantic proximity Read ↗

[Analysis of clinical phenotypes and GJB2 gene mutations in families affected with hearing loss from southern Zhejiang].Semantic proximity Read ↗

GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment.Semantic proximity Read ↗

[The sequencing analyze of 915 newborn with GJB2 heterozygous mutation in Beijing].Semantic proximity Read ↗

[The effects of newborn genetic screening for GJB2 and hearing follow-ups].Semantic proximity Read ↗

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