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Zebrafish ciliopathy screen plus human mutational analysis identifies C21orf59 and CCDC65 defects as causing primary ciliary dyskinesia

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第一作者: Austin-Tse,C.
作者单位: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, United [1] Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, United States [2] Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases [3] Department of Pediatrics, Stanford University, Stanford, CA 94304, United States [4] Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN [5] Department of Pathology, Laboratory Medicine, University of North Carolina, Chapel Hill, NC 27599 [6] Department of Pediatrics, University of Michigan, Ann Arbor, MI 48109, United States [7] Cystic Fibrosis/Pulmonary Research and Treatment Center, Chapel Hill, NC 27599, United States [8] Nephrology Division, Massachusetts General Hospital, Charlestown, MA 02129, United States [9] Department of General Pediatrics, University Children's Hospital Muenster [10] Division of Pulmonary and Critical Care, Washington University School of Medicine, St. Louis, MO [11] Children's Hospital, University of Washington, Seattle, WA 98105, United States [12] Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, ON M5G 1X8 [13] Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC 27599 [14] Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115 [15] Boulder Laboratory for 3-D Electron Microscopy of Cells, Department of Molecular, Cellular and [16] Department of Molecular, Microbial and Structural Biology, University of Connecticut Health Center [17] Germany [18]
发布时间 2018-07-27
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The American Journal of Human Genetics

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