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Article

Correlation between audiometric data and the 35delG mutation in ten patients.

Brazilian journal of otorhinolaryngology - 1 Jan 2000

Belintani Piatto Vânia, Vasques Moreira Otávio Augusto, Orate Menezes da Silva Magali Aparecida, Victor Maniglia José, Coimbra Pereira Márcio, Sartorato Edi Lúcia

Abstract excerpt

UNLABELLED: Mutations in the connexin 26 gene seem to be extremely common in non-syndromic hereditary deafness genesis, especially the 35delG, but there are still only a few studies that describe the audiometric characteristics of patients with these mutations. AIM: to analyze the audiometric characteristics of patients with mutations in the connexin 26 gene in order to outline genotype-phenotype correlation....

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Identifiers

PMID: 18278224
DOI: 10.1016/S1808-8694(15)31174-5
PMCID: PMC9450577

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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