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 journal › Article

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 journal › Article

Di Fabio, R, Tessa, A, Simons, EJ, Santorelli, FM, Casali, C, Serrao, M, Pierelli, F & Bonifati, V 2010, 'Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation', Parkinsonism and Related Disorders, vol. 16, no. 7, pp. 484-485. https://doi.org/10.1016/j.parkreldis.2010.05.001
Di Fabio R, Tessa A, Simons EJ, Santorelli FM, Casali C, Serrao M et al. Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation. Parkinsonism and Related Disorders. 2010 Aug;16(7):484-485. https://doi.org/10.1016/j.parkreldis.2010.05.001
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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