Mitochondrial dna variants observed in alzheimer disease and parkinson disease patients

Academic Article

Abstract

  • Mitochondrial DNA (mtDNA) variants associated with Alzheimer disease (AD) and Parkinson disease (PD) were sought by restriction endonuclease analysis in a cohort of 71 late-onset Caucasian patients. A tRNA gene variant at nucleotide pair (np) 4336 that altered a moderately conserved nucleotide was present in 9/173 (5.2%) of the patients surveyed but in only 0.7% of the general Caucasian controls. One of these patients harbored an additional novel 12S rRNA 5-nucleotide insertion at np 956-965, while a second had a missense variant at np 3397 that converted a highly conserved methionine to a valine. This latter mutation was also found in an independent AD + PD patient, as was a heteroplasmic 16S rRNA variant at np 3196. Additional studies will be required to determine the significance, if any, of these mutations. © 1993 Academic Press. All rights reserved. Gln
  • Authors

    Published In

  • Genomics  Journal
  • Digital Object Identifier (doi)

    Author List

  • Shoffner JM; Brown MD; Torroni A; Lott MT; Cabell MF; Mirra SS; Beal MF; Yang CC; Gearing M; Salvo R
  • Start Page

  • 171
  • End Page

  • 184
  • Volume

  • 17
  • Issue

  • 1