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Article

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.

International journal of pediatric otorhinolaryngology - 1 Sept 2010

Nahili Halima, Charif Majida, Boulouiz Redouane, Bounaceur Safaa, Benrahma Houda, Abidi Omar, Chafik Abdelaziz, Rouba Hassan, Kandil Mostafa, Barakat Abdelhamid

Abstract excerpt

UNLABELLED: Mutations in mitochondrial DNA (mtDNA), especially the A1555G transition in the 12S rRNA gene, are one of the causes of both aminoglycoside-induced and non-syndromic sensorineural hearing loss. OBJECTIVE: The aim of this study was to determine the prevalence of the A1555G mitochondrial mutation in Moroccan patients. METHODS: We performed molecular characterization by PCR-RFLP and direct sequencing of...

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

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Identifiers

PMID: 20637512
DOI: 10.1016/j.ijporl.2010.06.008

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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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