No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

Podobne knjige/članki

• Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.
  od: Brice, A, et al.
  Izdano: (1993)
• De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.
  od: Dumanchin, C, et al.
  Izdano: (1998)
• Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.
  od: Campion, D, et al.
  Izdano: (1999)
• No effect of the α1-antichymotrypsin A allele in Alzheimer's disease
  od: Didierjean, O, et al.
  Izdano: (1997)
• Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update
  od: Raux, G, et al.
  Izdano: (2005)