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Article

An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population.

International journal of pediatric otorhinolaryngology - 1 Jun 2017

Ghasemnejad Tohid, Shekari Khaniani Mahmoud, Zarei Fatemeh, Farbodnia Mina, Mansoori Derakhshan Sima

Abstract excerpt

Autosomal-recessive genes are responsible for about 80% of the hereditary non-syndromic hearing loss (NSHL) cases. In Iran, due to consanguineous marriages, NSHL is the second most frequent disability after intellectual disability, occurring one in 16 individuals. Enormous heterogeneity in the genetic pathology of hearing loss causes a major challenge in identification of responsible genes. In Iran, GJB2 is...

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Identifiers

PMID: 28483220
DOI: 10.1016/j.ijporl.2017.04.007

Genes

GJB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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