HSP60 is a rare cause of hereditary spastic paraparesis, but may act as a genetic modifier

Neurology. 2008 May 6;70(19):1717-8. doi: 10.1212/01.wnl.0000311395.31081.70.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adolescent
  • Adult
  • Chaperonin 60 / genetics*
  • Chromosome Disorders / genetics
  • DNA Mutational Analysis
  • Female
  • Gene Frequency / genetics
  • Genes, Dominant / genetics
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Genotype
  • Humans
  • Male
  • Mutation / genetics*
  • Pedigree
  • Spastic Paraplegia, Hereditary / genetics*
  • Spastic Paraplegia, Hereditary / metabolism*
  • Spastic Paraplegia, Hereditary / physiopathology
  • Spastin

Substances

  • Chaperonin 60
  • Genetic Markers
  • Adenosine Triphosphatases
  • Spastin
  • SPAST protein, human