...
机译:扩大的CTG重复标定了强直性营养不良患者组织中异常CpG甲基化的边界
Genetics and Genome Biology and;
Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA,;
Genetics and Genome Biology and|Inserm U781, Hôpital Necker-Enfants Malades, Paris 75015, France,;
Genetics and Genome Biology and|Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada M5G 1L7,|Department of Obstetrics and Gynecology, The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Toronto, Ontario, Canada and|Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada;
Inserm U781, Hôpital Necker-Enfants Malades, Paris 75015, France,;
Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA,;
机译:扩展的CTG重复标定了强直性营养不良患者组织中异常CpG甲基化的边界。
机译:具有扩大的CTG重复序列的人类强直性肌营养不良区转基因小鼠表现出肌肉和大脑异常。
机译:MSH3错配修复基因的多态性与1型强直性营养不良患者血液DNA中扩增的CTG重复序列的体细胞不稳定性水平相关
机译:肌动态营养不良和心脏传导系统异常:医师意识如何影响患者结果?
机译:1型强直性营养不良中的DNA复制和与疾病相关的三核苷酸重复不稳定性。
机译:扩大的CTG重复标定了强直性营养不良患者组织中异常CpG甲基化的边界
机译:扩大的CTG重复标定了强直性营养不良患者组织中异常CpG甲基化的边界