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Article

Mutations in the connexin 29 gene are not a major cause of nonsyndromic hearing impairment in India.

Genetic testing and molecular biomarkers - 1 Aug 2010

Ramchander Puppala Venkat, Panda Khirod Chandra, Panda Ashok Kumar

Abstract excerpt

Mutations in the GJC3 gene are known to cause nonsyndromic hearing impairment (NSHI). In this study, we screened for mutations in the connexin 29 (Cx29) gene in peripheral blood collected from patients with NSHI. DNA was extracted from peripheral blood cells of 123 NSHI patients and 127 normal-hearing control subjects. Coding regions of Cx29 were amplified by polymerase chain reaction using primer pairs flanking...

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Identifiers

PMID: 20632892
DOI: 10.1089/gtmb.2010.0026

Genes

GJC3

Variants

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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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