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Article

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Genetic testing and molecular biomarkers - 1 Apr 2012

Montazer Zohour Mostafa, Tabatabaiefar Mohammad Amin, Dehkordi Fatemeh Azadegan, Farrokhi Effat, Akbari Mohammad Taghi, Chaleshtori Morteza Hashemzadeh

Abstract excerpt

Hereditary hearing impairment (HI) is a genetically heterogeneous disorder caused by mutations either in nuclear DNA (nDNA) or in mitochondrial DNA (mtDNA). The nDNA mutations account for the majority of prelingual nonsyndromic HI (NSHI). The present survey was conducted to screen for known patho...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22077646
DOI: 10.1089/gtmb.2011.0176

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22077646-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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