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Article

Molecular investigation in children candidates and submitted to cochlear implantation.

Brazilian journal of otorhinolaryngology - 1 Jan 2000

Bernardes Raquel, Bortoncello Silvana, Christiani Thalita Vitachi, Sartorato Edi Lúcia, Silva Rodrigo César e, Porto Paulo R Cantanhede

Abstract excerpt

AIM: Recent progresses in molecular biology have been made in the diagnosis of sensorineural hearing loss. The high prevalence of a connexin 26 gene mutation, and its easy identification have made the diagnosis possible. The most frequent gene mutation is called 35delG. The purpose of this study was to evaluate the prevalence of 35delG mutation in children submitted to cochlear implantation who had severe and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 17119768
DOI: 10.1016/s1808-8694(15)30965-4
PMCID: PMC9443549

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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