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 journalArticle

6 Citations (Scopus)
Original languageEnglish
Pages (from-to)484-485
Number of pages2
JournalParkinsonism and Related Disorders
Volume16
Issue number7
DOIs
Publication statusPublished - Aug 2010

Keywords

  • Frontotemporal dementia
  • GRN
  • Mutation
  • Parkinsonism
  • Progranulin

ASJC Scopus subject areas

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

Cite this

Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation. / Di Fabio, Roberto; Tessa, Alessandra; Simons, Erik J.; Santorelli, Filippo M.; Casali, Carlo; Serrao, Mariano; Pierelli, Francesco; Bonifati, Vincenzo.

In: Parkinsonism and Related Disorders, Vol. 16, No. 7, 08.2010, p. 484-485.

Research output: Contribution to journalArticle

Di Fabio, Roberto ; Tessa, Alessandra ; Simons, Erik J. ; Santorelli, Filippo M. ; Casali, Carlo ; Serrao, Mariano ; Pierelli, Francesco ; Bonifati, Vincenzo. / Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation. In: Parkinsonism and Related Disorders. 2010 ; Vol. 16, No. 7. pp. 484-485.
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