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A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.
Sineni, Claire J; Yildirim-Baylan, Muzeyyen; Guo, Shengru; Camarena, Vladimir; Wang, Gaofeng; Tokgoz-Yilmaz, Suna; Duman, Duygu; Bademci, Guney; Tekin, Mustafa.
Affiliation
  • Sineni CJ; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue BRB-610 (M-860), Miami, FL, USA.
  • Yildirim-Baylan M; Department of Otorhinolaryngology, Dicle University School of Medicine, Diyarbakir, Turkey.
  • Guo S; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue BRB-610 (M-860), Miami, FL, USA.
  • Camarena V; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue BRB-610 (M-860), Miami, FL, USA.
  • Wang G; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue BRB-610 (M-860), Miami, FL, USA.
  • Tokgoz-Yilmaz S; Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Duman D; Department of Audiology, Ankara University Health Sciences Faculty, Ankara, Turkey.
  • Bademci G; Department of Audiology, Ankara University Health Sciences Faculty, Ankara, Turkey.
  • Tekin M; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue BRB-610 (M-860), Miami, FL, USA.
Hum Genet ; 138(10): 1071-1075, 2019 Oct.
Article in En | MEDLINE | ID: mdl-31175426
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Variation / Genetic Predisposition to Disease / Deafness / Claudins / Genetic Association Studies / Genes, Recessive Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2019 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Variation / Genetic Predisposition to Disease / Deafness / Claudins / Genetic Association Studies / Genes, Recessive Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 2019 Type: Article Affiliation country: United States