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

Παρόμοια τεκμήρια

• No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
  ανά: Campion, D, κ.ά.
  Έκδοση: (1996)
• Phenotypical difference of Amyloid Precursor Protein (APP) V717L mutation in Japanese family
  ανά: Abe, Masao, κ.ά.
  Έκδοση: (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
  ανά: Ancolio, K., κ.ά.
  Έκδοση: (1999)
• APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease
  ανά: Schellenberg, Gerard D., κ.ά.
  Έκδοση: (1991)
• Amyloid Precursor Protein (APP) and GABAergic Neurotransmission
  ανά: Tang, Bor Luen
  Έκδοση: (2019)