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Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment.
Wesdorp, Mieke; van de Kamp, Jiddeke M; Hensen, Erik F; Schraders, Margit; Oostrik, Jaap; Yntema, Helger G; Feenstra, Ilse; Admiraal, Ronald J C; Kunst, Henricus P M; Tekin, Mustafa; Kanaan, Moien; Kremer, Hannie; Pennings, Ronald J E.
Affiliation
  • Wesdorp M; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; The Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud Univers
  • van de Kamp JM; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Hensen EF; Department of Otolaryngology- Head and Neck Surgery, VU University Medical Center, Amsterdam, The Netherlands.
  • Schraders M; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Oostrik J; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Yntema HG; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Feenstra I; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Admiraal RJC; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Kunst HPM; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Tekin M; Hussman Institute for Human Genetics and Departments of Human Genetics and Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Kanaan M; Department of Biological Sciences, Bethlehem University, Bethlehem, Palestine.
  • Kremer H; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Human Genetics, Radboud University Medical Center, N
  • Pennings RJE; Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Hear Res ; 347: 56-62, 2017 04.
Article in En | MEDLINE | ID: mdl-28089734
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Frameshift Mutation / Codon, Nonsense / Hearing / Hearing Loss, Sensorineural / Microfilament Proteins Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Hear Res Year: 2017 Document type: Article Country of publication: Netherlands
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Frameshift Mutation / Codon, Nonsense / Hearing / Hearing Loss, Sensorineural / Microfilament Proteins Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Hear Res Year: 2017 Document type: Article Country of publication: Netherlands