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Article

Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.

Brazilian journal of otorhinolaryngology - 1 Jan 2000

Maniglia Luciano Pereira, Moreira Bruna Carolina Lemos, da Silva Magali Aparecida Orate Menezes, Piatto Vânia Belintani, Maniglia José Victor

Abstract excerpt

UNLABELLED: The A1555G mitochondrial mutation is the main alteration associated with aminoglycoside-induced deafness. AIM: to investigate the prevalence of the A1555G mutation in patients sensorineural hearing loss patients with and without aminoglycosides antibiotic use. MATERIAL AND METHOD: a study of 27 cases with deafness as the sample, and 100 neonates with normal hearing as the control group. DNA was...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 19082356
DOI: 10.1016/S1808-8694(15)31384-7
PMCID: PMC9445927

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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