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Article

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.

Journal of human genetics - 1 Oct 2010

Mahdieh Nejat, Rabbani Bahareh, Wiley Susan, Akbari Mohammad Taghi, Zeinali Sirous

Abstract excerpt

Hearing loss (HL) is the most prevalent sensory defect affecting 1 in 500 neonates. Genetic factors are involved in half of the cases. The extreme heterogeneity of HL makes it difficult to analyze and determine the accurate genetic causes of the impairment. Up to now, 10 genes, namely, GJB2, GJB6, SLC26A4, TECTA, PJVK, Col11A2, Myo15A, TMC1, RDX and microRNA (miR-183), have been studied in an Iranian population....

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Source

Identifiers

PMID: 20739942
DOI: 10.1038/jhg.2010.96

Genes

GJB2
TECTA
GJB6
PJVK
RDX
TMC1

Provenance

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Source receipt: pubmed, retrieved 7 Sept 2026.

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