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机译:家族性肌萎缩性侧索硬化症伴额颞叶痴呆与染色体9p13.2–21.3上的基因座相关
Department of Neurology King's College London School of Medicine Departments of;
Neurology and;
Molecular and Medical Genetics Institute of Psychiatry London UK;
Davee Department of Neurology and Clinical Neurosciences and;
Department of Cell and Molecular Biology Northwestern University Feinberg School of Medicine Chicago IL USA;
Department of Neurology and;
Department of Neuropathology Radboud University Medical Centre Nijmegen and Departments of;
Neuropathology;
Neurogenetics and;
Neurology Academic Medical Centre Amsterdam The Netherlands;
ALS; FTD; genetic linkage locus;
机译:具有额定仪性痴呆的家族肌萎缩侧面硬化症与染色体9p13.2-21.3上的轨迹有关
机译:家族性肌萎缩性侧索硬化症与额颞痴呆与染色体9q21-q22的联系。
机译:肌萎缩性侧索硬化:C9ORF72中的六核苷酸重复扩增将肌萎缩性侧索硬化和额颞痴呆联系起来。
机译:MARDI-TOF MS和FT-ICR MS的家族性肌萎缩外硬化相关交联Cu,Zn超氧化物歧化酶(SOD1)的分析
机译:家族性肌营养的外侧硬化剂,重点在C9ORF72己核苷酸GGGGCC重复膨胀相关的ALS与额定态痴呆
机译:在C9ORF72的非编码区扩大GGGGCC六核苷酸重复导致染色体9p联额颞叶痴呆和肌萎缩性侧索硬化
机译:具有额定仪性痴呆的家族肌萎缩侧面硬化症与染色体9p13.2-21.3上的轨迹有关