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Deletion of MAP2K2/MEK2: A novel mechanism for a RASopathy?

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第一作者: Nowaczyk,M.J.M.
作者单位: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, United [1] Children's Hospital Los Angeles, Departments of Pathology and Pediatrics, Keck School of Medicine [2] Institute of Human Genetics, Heidelberg University, Heidelberg, Germany [3] Department of Pediatrics, McMaster University, Hamilton, Canada [4] Department of Pathology and Laboratory Medicine, Medical Genetics Institute, Cedars-Sinai Medical [5] Department of Pediatrics, University of California, San Francisco, CA, United States [6] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States [7] Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada, Department [8] Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia, Department [9] Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada [10]
发布时间 2014-04-03
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Clinical Genetics: An International Journal of Genetics in Medicine

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