Detection of the presenilin 1 gene mutation (M139T) in early-onset familial Alzheimer disease in Spain

Neurosci Lett. 2001 Feb 23;299(3):239-41. doi: 10.1016/s0304-3940(01)01498-7.

Abstract

In a family with early-onset Alzheimer disease (EOAD) from Spain we found a mutation in the presenilin 1 (PS1) gene that predicts a methionine-to-threonine change at the PS1 residue 139 (M139T). This mutation was previously reported in a independent French family. The age of onset of the disease was similar in the affected members from both families, suggesting a specific age of expression (range 47-50 years). The detection of the M139T mutation in an independent EOAD family strongly supports the pathogenicity of this mutation in familial Alzheimer disease (AD).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / genetics*
  • Brain / pathology
  • Brain / physiopathology
  • Chromosomes, Human, Pair 14 / genetics
  • DNA Mutational Analysis
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Pedigree
  • Point Mutation / genetics*
  • Presenilin-1
  • Spain / epidemiology

Substances

  • Membrane Proteins
  • PSEN1 protein, human
  • Presenilin-1