Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation

J Neurol Neurosurg Psychiatry. 2009 Nov;80(11):1297-8. doi: 10.1136/jnnp.2008.169383.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Atrophy / complications
  • Atrophy / pathology
  • Brain / pathology*
  • Central Nervous System Diseases / genetics*
  • Central Nervous System Diseases / pathology*
  • Dementia / complications
  • Dementia / pathology
  • Female
  • Frameshift Mutation*
  • Functional Laterality
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Middle Aged
  • Paresis / complications
  • Paresis / pathology
  • Parkinsonian Disorders / complications
  • Parkinsonian Disorders / pathology
  • Phenotype
  • Progranulins
  • Syndrome

Substances

  • GRN protein, human
  • Intercellular Signaling Peptides and Proteins
  • Progranulins