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Article

GJB2 sequencing in deaf and profound sensorineural hearing loss children.

Otolaryngologia polska = The Polish otolaryngology - 30 Jun 2016

Mielczarek Marzena, Zakrzewska Anna, Olszewski Jurek

Abstract excerpt

INTRODUCTION: GJB2 mutations are the most frequent reason of genetic congenital hearing loss. The aim of the study was to assess the prevalence of GJB2 mutations in the deaf and profound hearing loss children. MATERIAL AND METHODS: The material of the study was a group of 61 patients divided into two groups. Group I - 35 deaf or with profound sensorineural hearing loss children (the pupils of the deaf and hard of...

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Source

Identifiers

PMID: 27386929
DOI: 10.5604/00306657.1199992

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.

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