Spectrum and frequency of connexin 26 & connexin 30 gene mutations in patients with congenital hearing loss from Ladakh India
Author:
Funder
Council of Scientific and Industrial Research, India
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference23 articles.
1. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among non-syndromic hearing loss patients in eastern part of India;Adhikary;Gene,2015
2. A high risk registry to find congenital deafness;Bergstrom;Otolaryngol clinics North America June,1971
3. Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment;Bhalla;Biochem. Biophys. Res. Commun.,2009
4. A genotype-phenotype correlation for GJB2 (connexin 26) deafness;Cryns;J. Med. Genet.,2004
5. Connexins and gap junctions in the inner ear;Forge;Audiology and Neurotology,2002
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