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Article

Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.

International journal of pediatric otorhinolaryngology - 1 Mar 2012

Minárik Gabriel, Tretinárová Denisa, Szemes Tomáš, Kádasi Ludevít

Abstract excerpt

OBJECTIVES: Non-syndromic hearing loss is one of the most common genetically determined diseases in human. The incidence is approximately 1:700 and most of the cases are caused by mutations in specific locus - DFNB1, which contains two genes -GJB2 and GJB6. For the GJB2 gene following mutations a...

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Source

Identifiers

PMID: 22281373
DOI: 10.1016/j.ijporl.2011.12.020

Genes

GJB6
GJB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22281373-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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