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Article

Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.

International journal of pediatric otorhinolaryngology - 1 Oct 2018

Moassass Faten, Al-Halabi Bassel, Nweder Mohamad Sayah, Al-Achkar Walid

Abstract excerpt

OBJECTIVE: Hearing loss is a common sensory disorder, and at least 50% of cases are due to a genetic etiology. Several mitochondrial DNA mutations (mtDNA) have been reported to be associated with nonsyndromic hearing loss (NSHL) in different population. However, There is no previous available data about the frequency of mtDNA mutations as etiology for deafness in Syrian. The aim of present study is to investigate...

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

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Source

Identifiers

PMID: 30173967
DOI: 10.1016/j.ijporl.2018.07.028

Genes

GJB2

Provenance

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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