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Article

Mitochondrial mutations in non-syndromic hearing loss at UAE.

International journal of pediatric otorhinolaryngology - 1 Nov 2020

Mohamed Walaa Kamal Eldin, Arnoux Marc, Cardoso Thyago H S, Almutery Abdullah, Tlili Abdelaziz

Abstract excerpt

INTRODUCTION: Hearing loss (HL) is a common sensory disorder over the world, and it has been estimated that genetic etiology is involved in more than 50% of the cases in developed countries. Both nuclear and mitochondrial genes were reported as responsible for hereditary HL. Mitochondrial mutations leading to HL have so far been reported in the MT-RNR1 gene, mitochondrially encoded 12S rRNA. METHODS: To study the...

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Identifiers

PMID: 32871514
DOI: 10.1016/j.ijporl.2020.110286

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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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