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Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene

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第一作者: Chanprasert,S.
作者单位: The Research Institute, Nationwide Children's Hospital, Columbus, OH, United States [1] Hospital La Paz, Madrid, Spain [2] Division of Medical Genetics, McGill University, Montreal, Canada [3] Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States [4] Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States, Department of [5] University of Texas Southwestern Medical Center, Dallas, TX, United States [6] Division of Medical Genetics, Department of Pediatrics, Stanford University School of Medicine [7] Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States, Texas [8] Division of Pediatric Neurology, Cincinnati Childrens Hospital Medical Center, Cincinnati, OH [9] Center for Gene Therapy, Research Institute, and Clinical Neuromuscular Laboratory, Nationwide [10] Department of Pathology, Children's Hospital and Medical Center, Omaha, NE, United States [11]
发布时间 2013-12-19
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Molecular genetics and metabolism

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