DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment
2011; Wiley; Volume: 79; Issue: 6 Linguagem: Inglês
10.1111/j.1399-0004.2010.01593.x
ISSN1399-0004
AutoresMA Tabatabaiefar, Fatemeh Alasti, Laleh Shariati, Effat Farrokhi, Erik Fransén, M. R. Noori‐Daloii, MH Chaleshtori, Guy Van Camp,
Tópico(s)Ear Surgery and Otitis Media
ResumoClinical GeneticsVolume 79, Issue 6 p. 594-598 DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment MA Tabatabaiefar, MA Tabatabaiefar Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran Department of Medical Genetics, University of Antwerp, 2610, Antwerp, Belgium These authors contribute equally to this work.Search for more papers by this authorF Alasti, F Alasti Department of Medical Genetics, University of Antwerp, 2610, Antwerp, Belgium National Institute for Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran These authors contribute equally to this work. Current address: Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USASearch for more papers by this authorL Shariati, L Shariati Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IranSearch for more papers by this authorE Farrokhi, E Farrokhi Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IranSearch for more papers by this authorE Fransen, E Fransen Department of Medical Genetics, University of Antwerp, 2610, Antwerp, Belgium StatUa Center for Statistics, University of Antwerp, Antwerp, BelgiumSearch for more papers by this authorMR Nooridaloii, MR Nooridaloii Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IranSearch for more papers by this authorMH Chaleshtori, MH Chaleshtori Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IranSearch for more papers by this authorG Van Camp, Corresponding Author G Van Camp Department of Medical Genetics, University of Antwerp, 2610, Antwerp, BelgiumGuy Van CampDepartment of Medical GeneticsUniversity of AntwerpUniversiteitsplein 12610 WilrijkBelgiumTel.: +323 275 9762Fax: +323 275 9722e-mail: [email protected]Search for more papers by this author MA Tabatabaiefar, MA Tabatabaiefar Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran Department of Medical Genetics, University of Antwerp, 2610, Antwerp, Belgium These authors contribute equally to this work.Search for more papers by this authorF Alasti, F Alasti Department of Medical Genetics, University of Antwerp, 2610, Antwerp, Belgium National Institute for Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran These authors contribute equally to this work. Current address: Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USASearch for more papers by this authorL Shariati, L Shariati Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IranSearch for more papers by this authorE Farrokhi, E Farrokhi Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IranSearch for more papers by this authorE Fransen, E Fransen Department of Medical Genetics, University of Antwerp, 2610, Antwerp, Belgium StatUa Center for Statistics, University of Antwerp, Antwerp, BelgiumSearch for more papers by this authorMR Nooridaloii, MR Nooridaloii Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IranSearch for more papers by this authorMH Chaleshtori, MH Chaleshtori Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, IranSearch for more papers by this authorG Van Camp, Corresponding Author G Van Camp Department of Medical Genetics, University of Antwerp, 2610, Antwerp, BelgiumGuy Van CampDepartment of Medical GeneticsUniversity of AntwerpUniversiteitsplein 12610 WilrijkBelgiumTel.: +323 275 9762Fax: +323 275 9722e-mail: [email protected]Search for more papers by this author First published: 05 May 2011 https://doi.org/10.1111/j.1399-0004.2010.01593.xCitations: 16 Current address: Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA 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. 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An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet 1999: 8 (3): 409– 412. Citing Literature Volume79, Issue6June 2011Pages 594-598 ReferencesRelatedInformation
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