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The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.
Küçük Kurtulgan, Hande; Altuntas, Emine Elif; Yildirim, Malik Ejder; Özdemir, Öztürk; Bagci, Binnur; Sezgin, Ilhan.
Afiliação
  • Küçük Kurtulgan H; Department of Medical Genetics, Cumhuriyet University School of Medicine, Sivas, Turkey.
  • Altuntas EE; Department of ENT, Cumhuriyet University School of Medicine, Sivas, Turkey.
  • Yildirim ME; Department of Medical Genetics, Cumhuriyet University School of Medicine, Sivas, Turkey.
  • Özdemir Ö; Department of Medical Genetics, Çanakkale 18 Mart University, Çanakkale, Turkey.
  • Bagci B; Department of Nutrition and Dietetics, Cumhuriyet University School of Medicine, Sivas, Turkey.
  • Sezgin I; Department of Medical Genetics, Cumhuriyet University School of Medicine, Sivas, Turkey.
J Int Adv Otol ; 15(3): 373-378, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31846914
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Conexinas / Conexina 30 / Perda Auditiva Neurossensorial Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Conexinas / Conexina 30 / Perda Auditiva Neurossensorial Idioma: En Ano de publicação: 2019 Tipo de documento: Article