Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation

Roberto Di Fabio, Alessandra Tessa, Erik J. Simons, Filippo M. Santorelli, Carlo Casali, Mariano Serrao, Francesco Pierelli, Vincenzo Bonifati

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)484-485
Number of pages2
JournalParkinsonism and Related Disorders
Issue number7
Publication statusPublished - Aug 2010


  • Frontotemporal dementia
  • GRN
  • Mutation
  • Parkinsonism
  • Progranulin

ASJC Scopus subject areas

  • Geriatrics and Gerontology
  • Clinical Neurology
  • Neurology
  • Medicine(all)

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