Amyloid precursor protein mutation causes Alzheimer's disease in a Swedish family

Neurosci Lett. 1994 Feb 28;168(1-2):254-6. doi: 10.1016/0304-3940(94)90463-4.

Abstract

Since the report of a double mutation at codons 670 and 671 of the amyloid precursor protein (APP) gene identified in two Swedish families with clinically diagnosed Alzheimer's disease (AD), a carrier with dementia has died. Neuropathology confirmed the clinical diagnosis of AD. Genealogical investigations have confirmed that the two families are related to common founders. Two-point linkage analysis of the mutation versus the disease in the revised pedigree now gives a lod score of 7.62.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / pathology
  • Amyloid beta-Protein Precursor / genetics*
  • Brain / pathology*
  • Female
  • Genetic Carrier Screening
  • Genetic Linkage
  • Humans
  • Lod Score
  • Male
  • Middle Aged
  • Mutation*
  • Neurofibrillary Tangles / pathology
  • Organ Specificity
  • Sweden

Substances

  • Amyloid beta-Protein Precursor