机译:磷脂酶D3基因中罕见的编码变异会增加患阿尔茨海默氏病的风险
Department of Psychiatry, Washington University, 425 South Euclid Avenue, St. Louis, Missouri 63110. USA,Hope Center Program on Protein Aggregation and Neurodegeneration, Washington University 425 South Euclid Avenue, St. Louis, Missouri 63110, USA;
Department of Psychiatry, Washington University, 425 South Euclid Avenue, St. Louis, Missouri 63110. USA,Hope Center Program on Protein Aggregation and Neurodegeneration, Washington University 425 South Euclid Avenue, St. Louis, Missouri 63110, USA;
Department of Psychiatry, Washington University, 425 South Euclid Avenue, St. Louis, Missouri 63110. USA;
Department of Psychiatry, Washington University, 425 South Euclid Avenue, St. Louis, Missouri 63110. SA;
Department of Psychiatry, Washington University, 425 South Euclid Avenue, St. Louis, Missouri 63110. USA;
et al;
机译:在晚期但不是早发性阿尔茨海默氏病中, PLD3 i>中罕见的编码变体过多
机译:PLD3中的罕见变种增加了汉族中阿尔茨海默病的风险
机译:PLD3的罕见变体不会影响欧洲联合体队列中早发性阿尔茨海默氏病的风险
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:营养转运蛋白的稀有遗传变异:对药物反应和人类疾病的影响
机译:磷脂酶D3(PLD3)中的罕见编码变体赋予患阿尔茨海默氏病的风险
机译:磷脂酶D3基因中罕见的编码变异会增加患阿尔茨海默氏病的风险。