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Genotype-phenotype correlations
Original article
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment

Authors

  • Kevin T Booth Molecular Otolaryngology Renal Research Laboratories, Department of Otolaryngology, University of Iowa, Iowa City, Iowa, USA The Interdisciplinary Graduate Program in Molecular Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA PubMed articlesGoogle scholar articles
  • Kimia Kahrizi Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Islamic Republic of Iran PubMed articlesGoogle scholar articles
  • Hossein Najmabadi Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Islamic Republic of Iran PubMed articlesGoogle scholar articles
  • Hela Azaiez Molecular Otolaryngology Renal Research Laboratories, Department of Otolaryngology, University of Iowa, Iowa City, Iowa, USA PubMed articlesGoogle scholar articles
  • Richard JH Smith Molecular Otolaryngology Renal Research Laboratories, Department of Otolaryngology, University of Iowa, Iowa City, Iowa, USA The Interdisciplinary Graduate Program in Molecular Medicine, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Hela Azaiez and Professor Richard JH Smith, Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology- Head and Neck Surgery, University of Iowa, Iowa City IA 52242, USA; hela-azaiez{at}uiowa.edu, richard-smith{at}uiowa.edu
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Citation

Booth KT, Kahrizi K, Najmabadi H, et al
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment
Journal of Medical Genetics 2018;55:555-560.

Publication history

  • Received February 23, 2018
  • Revised April 3, 2018
  • Accepted April 7, 2018
  • First published April 27, 2018.
Online issue publication 
June 15, 2020

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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.