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A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss |
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| Authors: | Asl? S?rmac?,Seyra Erbek,Mingqian Huang,F. Ba?ak Cengiz,Suna Tokgö z-Y?lmaz,Hilal Ö zda?,Sevsen Kulaks?zo?lu,Haris Kokotas,Michael B. Petersen,Moien Kanaan,Zheng-Yi Chen,Xue Z. Liu,Stephan Zuchner,Nejat Akar |
| Affiliation: | 1 Dr. John T. Macdonald Department of Human Genetics, University of Miami, Miller School of Medicine, Miami, FL 33136, USA 2 John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, FL 33136, USA 3 Department of Otorhinolaryngology, Baskent University School of Medicine, Ankara 06490, Turkey 4 Eaton-Peabody Laboratory, Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston 02114, USA 5 Division of Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara 06100, Turkey 6 Biotechnology Institute, Ankara University, Ankara 06100, Turkey 7 Department of Ophthalmology, Selcuk University Meram School of Medicine, Konya 42080, Turkey 8 Department of Biochemistry, Baskent University School of Medicine, Konya 42080, Turkey 9 Department of Radiodiagnostics, Baskent University School of Medicine, Konya 42080, Turkey 10 Department of Genetics, Institute of Child Health, ‘Aghia Sophia’ Children's Hospital, Athens 11527, Greece 11 Department of Life Sciences, Bethlehem University, Bethlehem, Palestinian Authority 12 Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA 13 Department of Otorhinolaryngology, University of Miami, Miller School of Medicine, Miami, FL 33136, USA |
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