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Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (<i>CFH</i>) gene family.

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第一作者: Stuart,Cantsilieris
第一单位: Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195.
作者单位: Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195. [1] Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195.;Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195. [2] Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany. [3] Centre for Eye Research Australia, Department of Surgery (Ophthalmology), University of Melbourne, Royal Victorian Eye and Ear Hospital, East Melbourne, VIC 3002, Australia. [4] McDonnell Genome Institute at Washington University, St. Louis, MO 63108. [5] Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43205.;Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH 93053. [6] Department of Ophthalmology, Columbia University, New York, NY 10027.;Department of Pathology and Cell Biology, Columbia University, New York, NY 10027. [7] Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195; eee@gs.washington.edu.;Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195. [8]
DOI 10.1073/pnas.1717600115
PMID 29686068
发布时间 2021-05-14
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Proceedings of the National Academy of Sciences of the United States of America

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