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Article

Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations.

The Laryngoscope - 1 Apr 2011

Lipan Michael, Ouyang Xiaomei, Yan Denise, Angeli Simon, Du Li Lin, Liu Xue-Zhong

Abstract excerpt

OBJECTIVES: The aim of the study is to assess clinical characteristics of individuals with nonsyndromic sensorineural hearing loss (NSSNHL) with genetic mutations in GJB2 and/or GJB6. We describe and compare one group with biallelic mutations against a group of heterozygote mutation carriers. METHODS: A total of 350 patients between the ages of 3 months and 80 years referred to a tertiary care outpatient otology...

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

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Source

Open in PubMed Open full text

Identifiers

PMID: 21287563
DOI: 10.1002/lary.21422
PMCID: PMC3065787

Genes

GJB2
GJB6

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.

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