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Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age

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第一作者: Mercier,S.
作者单位: APHP, Centre de référence maladies neuromusculaires, Hendaye, France [1] APHP, Department of Histology, CHU Mondor, Creteil, France [2] APHP, Department of Neuropediatry, CHU Trousseau, Paris, France [3] Paris V University, Institut Cochin, INSERM U1016, Paris, France [4] Department of Genetics, CHU Clocheville, Tours, France [5] Department of Neurology, CHU Angers, Angers, France [6] Department of Genetics, CHU Morvan, Brest, France [7] Institute of Myology, CHU H?pital Pitié-Salpétrière, Paris, France [8] Depatrment of Pediatry, H?pital Yves Le Foll, Saint Brieuc, France [9] Department of Neuropathology, CHU Brest, Brest, France [10] Departmentof Medical Genetics, CLAD Ouest, CHU Rennes, Rennes, France [11] Paris V University, Institut Cochin, INSERM U1016, Paris, France, APHP, Department of Neuropediatry [12] Department of Genetics, CH Vannes, Vannes, France [13] Department of Genetics, CHU Jeanne de Flandres, Lille, France [14] Department of Molecular Genetics, CHU Pontchaillou, Rennes, France [15] Department of Neuropediatry, CHU Pellerin, Bordeaux, France [16] Department of Pediatry, CH C?te Basque, Bayonne, France [17] APHP, Department of Neuromuscular disorders, CHU Salpétrière, Paris, France [18] Department of Pediatry, CHU Strasbourg, Strasbourg, France [19] Department of Medical Genetics, CHU Nantes, France, Paris V University, Institut Cochin, INSERM [20] Department of Genetics, CHU Dijon, Dijon, France [21]
发布时间 2018-09-20
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European journal of human genetics: EJHG

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