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Article

BanI/D13S141/D13S175 represents a novel informative haplotype at the GJB2 gene region in the Iranian population.

Cellular and molecular neurobiology - 1 Jul 2011

Rezaei Halimeh, Vallian Sadeq

Abstract excerpt

Non-syndromic sensorineural hearing loss (NSHL) represents the most common cause of hearing loss in the Iranian patients. In view of the large numbers of mutations identified in GJB2, mutations analysis of the gene has been time-consuming and cost-ineffective. Alternatively, molecular markers that are highly linked to the GJB2 gene have proven to be useful in carrier detection and prenatal diagnosis of NSHL...

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Identifiers

PMID: 21484343
DOI: 10.1007/s10571-011-9683-4

Genes

GJB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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