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Article

[Nonsyndromic sensorineural deafness--analysis of etiology in relatives].

Medycyna wieku rozwojowego - 1 Jan 2000

Nowakowska-Szyrwinska Ewa, Sobieszczanska-Radoszewska Lucja

Abstract excerpt

We present the results of complex clinical examination of children affected with sensorineural hearing loss. The siblings (minimum two) were born from unaffected parents and came from twelve families. Molecular studies confirmed genetic background of hearing loss in 6 families and enabled identification of GJB2 mutations in investigated probants.

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Identifiers

PMID: 13130165

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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