Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference40 articles.
1. Genetic epidemiology of hearing impairment;Morton;Ann. NY Acad. Sci.,1991
2. Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis;Kikuchi;Anat. Embryol.,1995
3. Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness;Kelsell;Nature,1997
4. The role of connexins in human disease;Chang;Ear Hear.,2003
5. Non-syndromic, autosomal-recessive deafness;Petersenm;Clin. Genet.,2006
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2. A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing Impairment;Indian Journal of Otolaryngology and Head & Neck Surgery;2023-07-07
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