Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.

類似資料

• 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)
• Phenotypical difference of Amyloid Precursor Protein (APP) V717L mutation in Japanese family
  著者:: Abe, Masao, 等
  出版事項: (2012)
• Unusual phenotypic alteration of β amyloid precursor protein (βAPP) maturation by a new Val-715 → Met βAPP-770 mutation responsible for probable early-onset Alzheimer’s disease
  著者:: Ancolio, K., 等
  出版事項: (1999)
• Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)
  著者:: Nágela S. V. Nunes, 等
• APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease
  著者:: Schellenberg, Gerard D., 等
  出版事項: (1991)