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Article

Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.

International journal of pediatric otorhinolaryngology - 1 Jun 2012

Yazdanpanahi Nasrin, Chaleshtori Morteza Hashemzadeh, Tabatabaiefar Mohammad Amin, Noormohammadi Zahra, Farrokhi Effat, Najmabadi Hossein, Shahbazi Shirin, Hosseinipour Azam

Abstract excerpt

OBJECTIVE: Due to the fact that SLC26A4 has been suggested as the second cause of hearing loss (HL) in Iran as well as many other countries, obtaining more comprehensive information about SLC26A4 mutations can facilitate more efficient genetic services to the patients with hereditary hearing loss...

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Source

Identifiers

PMID: 22444735
DOI: 10.1016/j.ijporl.2012.02.056

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22444735-2026-09-04.1. Manifest publication-graph-cohort-2026-09-04.1.

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

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