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Article

Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss.

Archives of disease in childhood - 1 Sept 2011

Yoong Soo Y, Mavrogiannis Lampros A, Wright John, Fairley Lesley, Bennett Christopher P, Charlton Ruth S, Spencer Nick

Abstract excerpt

OBJECTIVE: To determine the clinical sensitivity of DFNB1 genetic testing (analysis of the connexin 26 gene GJB2) for non-syndromic sensorineural hearing loss (SNHL) in British Pakistani children and extend to a comparison with British White children and literature data. DESIGN: Retrospective cohort study. SETTING: City of Bradford, UK. PATIENTS: Overall, 177 children (152 families) were eligible; 147 children...

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Source

Identifiers

PMID: 21586435
DOI: 10.1136/adc.2010.209262

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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