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Article

Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.

Archives of otolaryngology--head & neck surgery - 1 Jan 2010

Kenna Margaret A, Feldman Henry A, Neault Marilyn W, Frangulov Anna, Wu Bai-Lin, Fligor Brian, Rehm Heidi L

Abstract excerpt

OBJECTIVES: To document the audiologic phenotype of children with biallelic GJB2 (connexin 26) mutations, and to correlate it with the genotype. DESIGN: Prospective, observational study. SETTING: Tertiary care children's hospital. PATIENTS: Infants and children with sensorineural hearing loss (SN...

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Source

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Identifiers

PMID: 20083784
DOI: 10.1001/archoto.2009.202
PMCID: PMC4528189

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20083784-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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