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

Ítems similars

• No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
  per: Campion, D, et al.
  Publicat: (1996)
• Phenotypical difference of Amyloid Precursor Protein (APP) V717L mutation in Japanese family
  per: Abe, Masao, et al.
  Publicat: (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
  per: Ancolio, K., et al.
  Publicat: (1999)
• Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)
  per: Nágela S. V. Nunes, et al.
• APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease
  per: Schellenberg, Gerard D., et al.
  Publicat: (1991)