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Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: Clinical comparison of retroviral vectors and treatment plans

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第一作者: Candotti,F.
作者单位: Department of Biochemistry, Duke University, School of Medicine, Durham, NC, United States [1] Genetics and Molecular Biology Branch, National Human Genome Research Institute, National [2] Department of Biostatistics, School of Public Health, UCLA, Los Angeles, CA, United States [3] Department of Microbiology, Immunology and Molecular Genetics, University of California, Los [4] Department of Pediatrics, Section of Allergy and Immunology, Texas Children's Hospital, Houston, TX [5] Hematology/Oncology, Dell Children's Medical Center of Central Texas, Austin, TX, United States [6] Department of Internal Medicine, University of California, Davis School of Medicine, Sacramento, CA [7] Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA, United States [8] Immune Deficiency Foundation, Towson, MD, United States [9] Department of Pediatrics, Children's Hospital Los Angeles, University of Southern California, Los [10] Department of Pathology and Laboratory Medicine, UCLA David Geffen School of Medicine, Los Angeles [11] Hematologic Diseases Section, National Cancer Institute, NIH, Bethesda, MD, United States [12] Arizona Allergy Associates, Scottsdale, AZ, United States [13] Molecular and Clinical Hematology Branch, National Institute of Diabetes and Digestive and Kidney [14] Department of Pediatrics, Stanford School of Medicine, Stanford, CA, United States [15] Molecular Biology Interdepartmental PhD Program, UCLA David Geffen School of Medicine, Los Angeles [16] Division of Hematology, Center for Cellular and Molecular Therapeutics, Children's Hospital of [17] Division of Infectious Diseases, Department of Medicine, UCLA David Geffen School of Medicine, Los [18]
发布时间 2013-11-20
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Blood: The Journal of the American Society of Hematology

Blood

2012年120卷18期

3635-3646页

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