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Article

Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in the MTRNR1 Gene.

The Laryngoscope - 1 Feb 2025

Gallo-Terán Jaime, Salomón-Felechosa Cristina, González-Aguado Rocío, Onecha Esther, Fontalba Ana, Del Castillo Ignacio, Morales-Angulo Carmelo

Abstract excerpt

OBJECTIVE: Mutations in the MTRNR1 gene of mitochondrial DNA are associated with non-syndromic hearing loss and increased susceptibility to aminoglycoside ototoxicity. The aim of our study was to determine the clinical characteristics of sensorineural hearing loss caused by the m.1555A>G mutation in MTRNR1. METHODS: An observational retrospective study of the m.1555A>G mutation was conducted in patients with...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 39323315
DOI: 10.1002/lary.31796
PMCID: PMC11725701

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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