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Article

Incidence of the del35G/GJB2 mutation in Croatian newborns with hearing impairment.

Medical science monitor : international medical journal of experimental and clinical research - 1 Nov 2005

Medica Igor, Rudolf Gorazd, Prpić Igor, Stanojević Milan, Peterlin Borut

Abstract excerpt

BACKGROUND: The de135G mutation in the GJB2 gene is the most common cause of prelingual deafness. The mutation frequency has so far been estimated either by testing symptomatic children or adults, or by carrier testing of the general population. The purpose of our study was to establish the incid...

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Source

Identifiers

PMID: 16258398

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16258398-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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