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Article

Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family.

Gene - 25 May 2013

Ramzan Khushnooda, Al-Owain Mohammed, Allam Rabab, Berhan Amal, Abuharb Gheid, Taibah Khalid, Imtiaz Faiqa

Abstract excerpt

Hearing loss is one of the most common sensory disorders in humans and has a genetic cause in 50% of the cases. Our recent studies indicate that nonsyndromic hearing loss (NSHL) in the Saudi Arabian population is genetically heterogeneous and is not caused by mutations in GJB2 and GJB6, the most common genes for deafness in various populations worldwide. Identification of the causative gene/mutation in affected...

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Source

Identifiers

PMID: 23510777
DOI: 10.1016/j.gene.2013.03.042

Genes

GIPC3
GJB2
GJB6

Variants

Provenance

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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