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Article

Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in Austria.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology - 1 Oct 2007

Ramsebner Reinhard, Lucas Trevor, Schoefer Christian, Ludwig Martin, Baumgartner Wolf-Dieter, Wachtler Franz J, Kirschhofer Karin, Frei Klemens

Abstract excerpt

OBJECTIVE: To analyze the prevalence and importance of the maternally inherited A1555G mutation in the 12S rRNA gene in the Austrian population. STUDY DESIGN: Investigation for mutations of genetically affected familial and sporadic cases of hearing impairment (HI), including analyses of audiometric data. SETTING: Teaching hospital, tertiary referral center. PATIENTS: Forty-five familial and 77 sporadic cases of...

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Identifiers

PMID: 17955603

Genes

GJB2

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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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