A novel silent variant at codon 711 and a variant at codon 708 of the APP sequence detected in Spanish Alzheimer and control cases

Neurosci Lett. 1993 Feb 5;150(1):33-4. doi: 10.1016/0304-3940(93)90101-p.

Abstract

Pathogenic mutations have been identified in exons 16 and 17 of the beta-amyloid precursor protein (APP) gene in some cases of early onset Alzheimer's disease. Screening of these exons in a number of familial and sporadic cases of Alzheimer's disease in Spain, resulted in the identification of a novel silent variant at codon 711 whose relevance to the AD pathogenesis remains unclear. The 708 variant was also detected in one of normal controls.

MeSH terms

  • Alzheimer Disease / genetics*
  • Amino Acid Sequence
  • Amyloid beta-Protein Precursor / genetics*
  • Codon
  • DNA / genetics
  • DNA / isolation & purification
  • Exons
  • Genetic Variation*
  • Humans
  • Mutation*
  • Reference Values
  • Spanien

Substances

  • Amyloid beta-Protein Precursor
  • Codon
  • DNA