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A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

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第一作者: Michael R,Bowl
第一单位: Medical Research Council Harwell Institute (Mammalian Genetics Unit and Mary Lyon Centre), Harwell, Oxfordshire, OX11 0RD, UK.
作者单位: Medical Research Council Harwell Institute (Mammalian Genetics Unit and Mary Lyon Centre), Harwell, Oxfordshire, OX11 0RD, UK. [1] King's College London, London, SE1 1UL, UK.;The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. [2] European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1 SD, UK. [3] The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. [4] Mouse Biology Program, University of California, Davis, California, 95618, USA. [5] CELPHEDIA, PHENOMIN, Institut Clinique de la Souris (ICS), 1 rue Laurent Fries, Illkirch-Graffenstaden, F-67404, France. [6] RIKEN BioResource Center, Tsukuba, Ibaraki, 305-0074, Japan. [7] The Centre for Phenogenomics, Toronto, Ontario, Canada, M5T 3H7.;The Hospital for Sick Children, Toronto, Ontario, Canada, M5G 1X8.;Canada and Mount Sinai Hospital, Toronto, Ontario, Canada, M5G 1X5. [8] Monterotondo Mouse Clinic, Italian National Research Council (CNR), Institute of Cell Biology and Neurobiology, I-00015, Monterotondo Scalo, Italy. [9] SKL of Pharmaceutical Biotechnology and Model Animal Research Center, Collaborative Innovation Center for Genetics and Development, Nanjing Biomedical Research Institute, Nanjing University, 210061, Nanjing, China. [10] IMPC, San Anselmo, California, 94960, USA. [11] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA. [12] The Centre for Phenogenomics, Toronto, Ontario, Canada, M5T 3H7.;The Hospital for Sick Children, Toronto, Ontario, Canada, M5G 1X8.;Canada and Mount Sinai Hospital, Toronto, Ontario, Canada, M5G 1X5.;Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA. [13] Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, 77030, USA. [14] Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health GmbH, Ingolstaedter Landstrasse 1, 85764, Neuherberg, Germany. [15] German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health GmbH, Ingolstaedter Landstrasse 1, 85764, Neuherberg, Germany. [16] CELPHEDIA, PHENOMIN, Institut Clinique de la Souris (ICS), 1 rue Laurent Fries, Illkirch-Graffenstaden, F-67404, France.;Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, 67404, Illkirch, France.;Centre National de la Recherche Scientifique, UMR7104, 67404, Illkirch, France.;Institut National de la Santé et de la Recherche Médicale, U964, 67404, Illkirch, France. [17] The Jackson Laboratory, Bar Harbor, Maine, 04609, USA. [18] Childrens' Hospital Oakland Research Institute, Oakland, California, 94609, USA. [19] Queen Mary University of London, London, WC1E 6BT, UK. [20] Medical Research Council Harwell Institute (Mammalian Genetics Unit and Mary Lyon Centre), Harwell, Oxfordshire, OX11 0RD, UK. s.brown@har.mrc.ac.uk. [21]
DOI 10.1038/s41467-017-00595-4
PMID 29026089
发布时间 2024-02-14
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