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Article

Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population.

Genetic testing and molecular biomarkers - 1 Dec 2014

Mojtabavi Naeini Marjan, Mesrian Tanha Hamzeh, Hashemzadeh Chaleshtori Morteza, Vallian Sadeq

Abstract excerpt

BACKGROUND AND AIMS: SLC26A4 gene mutations are the second currently identifiable genetic cause of autosomal recessive nonsyndromic hearing loss after GJB2 mutations. Because of the extensive size of the SLC26A4 gene and the variety of mutations, indirect diagnosis using linkage analysis has been suggested. Therefore, in this investigation three potential short tandem repeat (STR) markers related to this region...

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Identifiers

PMID: 25390158
DOI: 10.1089/gtmb.2014.0178
PMCID: PMC4250946

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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