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Article

Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.

Biochemical and biophysical research communications - 24 Feb 2006

Mkaouar-Rebai Emna, Tlili Abdelaziz, Masmoudi Saber, Louhichi Nacim, Charfeddine Ilhem, Ben Amor Mohamed, Lahmar Imed, Driss Nabil, Drira Mohamed, Ayadi Hammadi, Fakhfakh Faiza

Abstract excerpt

We explored the mitochondrial 12S rRNA and the tRNASer(UCN) genes in 100 Tunisian families affected with NSHL and in 100 control individuals. We identified the mitochondrial A1555G mutation in one out of these 100 families and not in the 100 control individuals. Members of this family harbouring...

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Source

Identifiers

PMID: 16406239
DOI: 10.1016/j.bbrc.2005.12.123

Genes

UCN
GJB2
GJB3
GJB6

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16406239-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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