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Article

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.

International journal of audiology - 1 Mar 2012

Khalifa Alkowari M, Girotto G, Abdulhadi K, Dipresa S, Siam R, Najjar N, Badii R, Gasparini P

Abstract excerpt

OBJECTIVE: This study reports results from the first survey of the genetic causes of nonsyndromic sensorineural hearing loss (NSHHL) in the Qatari population. DESIGN AND STUDY SAMPLES: Data were collected from 126 Qatari patients (58 males and 68 females) belonging to inbred families (56%), showing an autosomal recessive pattern of inheritance (96%). Fifty-three patients were less than 10 years old, 55 in the age...

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Source

Identifiers

PMID: 22103400
DOI: 10.3109/14992027.2011.625983

Genes

GJB6
GJB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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