Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations

Neurology. 2008 Jul 22;71(4):303; author reply 303-4. doi: 10.1212/01.wnl.0000320511.30222.dd.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Aphasia, Primary Progressive / genetics*
  • Aphasia, Primary Progressive / metabolism
  • Aphasia, Primary Progressive / physiopathology
  • Causality
  • DNA Mutational Analysis / standards
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing / standards
  • Genetic Variation / genetics
  • Genotype
  • Humans
  • Inheritance Patterns / genetics
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Mutation / genetics*
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / physiopathology
  • Norway
  • Parkinson Disease / genetics
  • Parkinson Disease / metabolism
  • Parkinson Disease / physiopathology
  • Protein-Serine-Threonine Kinases / genetics*
  • Risk Factors

Substances

  • Genetic Markers
  • LRRK2 protein, human
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Protein-Serine-Threonine Kinases