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Variants in CIB2 cause DFNB48 and not USH1J.
Booth, K T; Kahrizi, K; Babanejad, M; Daghagh, H; Bademci, G; Arzhangi, S; Zareabdollahi, D; Duman, D; El-Amraoui, A; Tekin, M; Najmabadi, H; Azaiez, H; Smith, R J.
Afiliação
  • Booth KT; Department of Otolaryngology, Head and Neck Surgery, Molecular Otolaryngology and Renal Research Laboratories, University of Iowa, Iowa City, IA, USA.
  • Kahrizi K; Interdisciplinary Graduate Program in Molecular Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
  • Babanejad M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Daghagh H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Bademci G; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Arzhangi S; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Zareabdollahi D; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Duman D; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • El-Amraoui A; Division of Pediatric Genetics, Ankara University School of Medicine, Ankara, Turkey.
  • Tekin M; Institut Pasteur, Génétique et Physiologie de l'Audition, Paris, France.
  • Najmabadi H; John P. Hussman Institute for Human Genomics, Dr. John T. Macdonald Foundation Department of Human Genetics, Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Azaiez H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Smith RJ; Department of Otolaryngology, Head and Neck Surgery, Molecular Otolaryngology and Renal Research Laboratories, University of Iowa, Iowa City, IA, USA.
Clin Genet ; 93(4): 812-821, 2018 04.
Article em En | MEDLINE | ID: mdl-29112224
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Ligação ao Cálcio / Predisposição Genética para Doença / Síndromes de Usher / Perda Auditiva Neurossensorial Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Ligação ao Cálcio / Predisposição Genética para Doença / Síndromes de Usher / Perda Auditiva Neurossensorial Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article