GJB2 mutations in Turkish patients with nonsyndromic hearing loss
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference29 articles.
1. GJB2 gene mutations causing familial hereditary deafness in Turkey;Bayazit;Int. J. Pediatr. Otorhinolaryngol.,2003
2. GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals;Baysal;J. Genet.,2008
3. Prevalence of the IVS1(+1)G→A and 35delG mutations in the GJB2 gene of Turkish patients with nonsyndromic hearing loss;Biyikli;Turk. J. Biol.,2012
4. The prevalence of gap junction protein Beta 2 (GJB2) mutations in non-syndromic sensorineural hearing loss in Cukurova region;Bozdogan;J. Int. Adv. Otol.,2015
5. Deafness induced by connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders;Chen;Biochem. Biophys. Res. Commun.,2014
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