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机译:鉴定Alzheimer疾病中中国人的罕见编码变体
Univ Calif San Francisco Dept Neurol Memory &
Aging Ctr San Francisco CA 94143 USA;
Univ Calif Berkeley Howard Hughes Med Inst Dept Mol &
Cell Biol Berkeley CA 94720 USA;
Univ Calif San Francisco Dept Neurol Memory &
Aging Ctr San Francisco CA 94143 USA;
Univ Calif Berkeley Howard Hughes Med Inst Dept Mol &
Cell Biol Berkeley CA 94720 USA;
Univ Calif San Francisco Dept Neurol Memory &
Aging Ctr San Francisco CA 94143 USA;
Univ Calif Los Angeles Dept Psychiat Los Angeles CA USA;
Univ Calif Los Angeles Dept Psychiat Los Angeles CA USA;
Univ Calif Los Angeles Dept Psychiat Los Angeles CA USA;
Univ Calif San Francisco Dept Neurol Memory &
Aging Ctr San Francisco CA 94143 USA;
Univ Calif San Francisco Dept Neurol Memory &
Aging Ctr San Francisco CA 94143 USA;
Univ Calif San Francisco Dept Neurol Memory &
Aging Ctr San Francisco CA 94143 USA;
TREM2; Alzheimer's disease; dementia; genetics; case report; Chinese; rare variant;
机译:鉴定Alzheimer疾病中中国人的罕见编码变体
机译:跨种族的荟萃分析对PLCG2,ABI3和TREM2中的罕见编码变异进行了支持
机译:PLCG2,ABI3和TREM2中罕见的编码变体均致癌在阿尔茨海默病中的微胶质介导的先天免疫力
机译:VariFunNet,一个集成的多尺度建模框架,用于研究全基因组关联研究中罕见的非编码变体的影响:应用于阿尔茨海默氏病
机译:阿尔茨海默氏病中线粒体DNA变体的鉴定和表征。
机译:在中国阿尔茨海默氏病患者中鉴定出TREM2中罕见的编码变异
机译:鉴定Alzheimer疾病的中国人稀有编码变体