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Alterations of the CIB2 calcium-and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

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第一作者: Riazuddin,S.
作者单位: Department of Biological Sciences, McMicken College of Arts and Sciences, University of Cincinnati [1] Allama Iqbal Medical College, Lahore, Pakistan [2] Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders [3] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States [4] Institute of Biotechnology, Baluchistan University of Information Technology, Quetta, Pakistan [5] Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill [6] Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad [7] Department of Physiology, University of Kentucky, Lexington, KY, United States [8] Division of Pediatric Otolaryngology/Head and Neck Surgery, Cincinnati Children's Hospital Medical [9] Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH [10] Institute of Biochemistry, University of Baluchistan, Quetta, Pakistan [11] Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, FL, United [12] Allama Iqbal Medical College, Lahore, Pakistan, University of Lahore, Lahore, Pakistan [13] Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH [14] National Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan [15]
发布时间 2013-11-20
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Nature Genetics

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