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Comertpay G

Turkey
Publications

P. [V27i; E114g] Compound Heterozygous State in Gjb2 Gene Could Be an Indicator of the Severity of Congenital Hearing Loss

Hearing loss (HL) is the most common sensory disorder, affecting all age groups, ethnicities, and genders. Several genes responsible for hearing loss are related to ion recycling and homeostasis in the inner ear. Mutations in GJB2 gene, the gene encoding gap junction protein connexin26 (Cx26), are most common detected in patients with congenital, r... Read More»

Tufan T, Erkoc MA, Yilmaz MB, Comertpay G and Alptekin D

Case Report: Otolaryngol (Sunnyvale) 2015, 5:209

DOI: 10.4172/2161-119X.1000209

Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article

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