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  • Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands

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Genotype-phenotype correlations
Original research
Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands

Authors

  • Hedwig M Velde Department of Otorhinolaryngology, Radboudumc, Nijmegen, The Netherlands Donders Institute for Brain Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Nienke C Homans Department of Otorhinolaryngology Head and Neck Surgery, Erasmus Medical Center, Rotterdam, The Netherlands PubMed articlesGoogle scholar articles
  • André Goedegebure Department of Otorhinolaryngology Head and Neck Surgery, Erasmus Medical Center, Rotterdam, The Netherlands PubMed articlesGoogle scholar articles
  • Cornelis P Lanting Department of Otorhinolaryngology, Radboudumc, Nijmegen, The Netherlands Donders Institute for Brain Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Ronald J E Pennings Department of Otorhinolaryngology, Radboudumc, Nijmegen, The Netherlands Donders Institute for Brain Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Hannie Kremer Donders Institute for Brain Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands Department of Otorhinolaryngology and Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Hannie Kremer, Department of Otorhinolaryngology and Department of Human Genetics, Radboudumc, Nijmegen, 6525 GA, Netherlands; Hannie.Kremer{at}radboudumc.nl
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Citation

Velde HM, Homans NC, Goedegebure A, et al
Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands
Journal of Medical Genetics 2023;60:1061-1066.

Publication history

  • Received January 5, 2023
  • Accepted April 16, 2023
  • First published May 10, 2023.
Online issue publication 
October 24, 2023

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© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.