A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease

Ann Genet. 1998;41(3):149-53.

Abstract

A search for mutations in exons 6, 7, 9 and 12 of the PS1 gene in four Mexican families with Early-Onset (36-40 years) Alzheimer Disease yielded the discovery in one family of a T-->C mismatch in exon 7 which correspond to nucleotide 760 of cDNA, leading to a Leu171Pro mutation. The pedigree analysis and the literature data strongly suggest an etiopathogenic relationship of the mutation with the disorder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Alzheimer Disease / genetics*
  • Amino Acid Substitution
  • Humans
  • Leucine
  • Membrane Proteins / genetics*
  • Mexico
  • Mutation, Missense*
  • Pedigree
  • Polymerase Chain Reaction
  • Presenilin-1
  • Proline

Substances

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