A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration

Neurology. 2000 May 23;54(10):2028-30. doi: 10.1212/wnl.54.10.2028.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Cerebral Cortex / pathology
  • Chromosomes, Human, Pair 17*
  • Diagnostic Imaging
  • Dopamine / metabolism
  • Exons / genetics
  • Globus Pallidus*
  • Homovanillic Acid / metabolism
  • Humans
  • Multiple System Atrophy / diagnosis
  • Multiple System Atrophy / genetics*
  • Mutation, Missense / genetics*
  • Phenotype
  • Striatonigral Degeneration / diagnosis
  • Striatonigral Degeneration / genetics*
  • Substantia Nigra*
  • gamma-Aminobutyric Acid / metabolism
  • tau Proteins / genetics*

Substances

  • tau Proteins
  • gamma-Aminobutyric Acid
  • Dopamine
  • Homovanillic Acid