Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease
研究孟德尔痴呆基因（APP、PSEN1、PSEN2、GRN、MAPT 和 PRNP）中罕见编码变异在晚发性阿尔茨海默病中的作用
期刊:Neurobiology of Aging
影响因子:3.5
doi:10.1016/j.neurobiolaging.2014.06.002
Sassi, Celeste; Guerreiro, Rita; Gibbs, Raphael; Ding, Jinhui; Lupton, Michelle K; Troakes, Claire; Al-Sarraj, Safa; Niblock, Michael; Gallo, Jean-Marc; Adnan, Jihad; Killick, Richard; Brown, Kristelle S; Medway, Christopher; Lord, Jenny; Turton, James; Bras, Jose; Morgan, Kevin; Powell, John F; Singleton, Andrew; Hardy, John
