Article info
Genotype-phenotype correlations
Original article
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment
- 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
Citation
Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment
Publication history
- Received February 23, 2018
- Revised April 3, 2018
- Accepted April 7, 2018
- First published April 27, 2018.
Online issue publication
July 24, 2018
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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.