Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)

Abstract

American Journal of Medical Genetics Part AVolume 140A, Issue 16 p. 1791-1794 Research Letter Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)† Rob W.J. Collin, Rob W.J. Collin Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorRobert J. Pauw, Robert J. Pauw Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorJeroen Schoots, Jeroen Schoots Department of Human Genetics, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorPatrick L.M. Huygen, Patrick L.M. Huygen Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorLies H. Hoefsloot, Lies H. Hoefsloot Department of Human Genetics, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorCor W.R.J. Cremers, Cor W.R.J. Cremers Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorHannie Kremer, Corresponding Author Hannie Kremer h.kremer@antrg.umcn.nl Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsDepartment of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Internal Postal Code 377, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.Search for more papers by this author Rob W.J. Collin, Rob W.J. Collin Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorRobert J. Pauw, Robert J. Pauw Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorJeroen Schoots, Jeroen Schoots Department of Human Genetics, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorPatrick L.M. Huygen, Patrick L.M. Huygen Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorLies H. Hoefsloot, Lies H. Hoefsloot Department of Human Genetics, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorCor W.R.J. Cremers, Cor W.R.J. Cremers Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsSearch for more papers by this authorHannie Kremer, Corresponding Author Hannie Kremer h.kremer@antrg.umcn.nl Department of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Nijmegen, The NetherlandsDepartment of Otorhinolaryngology, Radboud University Medical Center Nijmegen, Internal Postal Code 377, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.Search for more papers by this author First published: 11 July 2006 https://doi.org/10.1002/ajmg.a.31354Citations: 24 † How to cite this article: Collin RWJ, Pauw RJ, Schoots J, Huygen PLM, Hoefsloot LH, Cremers CWRJ, Kremer H. 2006. Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9). Am J Med Genet Part A 140A:1791–1794. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume140A, Issue1615 August 2006Pages 1791-1794 RelatedInformation