RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

類似資料

• APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease
  著者:: Schellenberg, Gerard D., 等
  出版事項: (1991)
• Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.
  著者:: Brice, A, 等
  出版事項: (1993)
• No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
  著者:: Campion, D, 等
  出版事項: (1996)
• Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's disease
  著者:: Bales, Kelly R., 等
  出版事項: (1999)
• The familial Alzheimer's disease APPV717I mutation alters APP processing and Tau expression in iPSC-derived neurons
  著者:: Muratore, Christina R., 等
  出版事項: (2014)