A novel MAPT mutation (P301T) associated with familial frontotemporal dementia

Eur J Neurol. 2007 Aug;14(8):e9-10. doi: 10.1111/j.1468-1331.2007.01763.x.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Akinetic Mutism / etiology
  • Akinetic Mutism / physiopathology
  • Base Sequence
  • Brain / pathology
  • Brain / physiopathology
  • Codon / genetics
  • Cognition Disorders / etiology
  • Cognition Disorders / physiopathology
  • DNA Mutational Analysis
  • Dementia / genetics*
  • Dementia / pathology
  • Dementia / physiopathology*
  • Family Health
  • Female
  • Gait Disorders, Neurologic / etiology
  • Gait Disorders, Neurologic / physiopathology
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Pedigree
  • Point Mutation
  • Spain
  • tau Proteins / genetics*

Substances

  • Codon
  • tau Proteins