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

2010-08-01

Parkinsonism & Related Disorders , Volume 16 - Issue 7 p. 484- 485

Additional Metadata
Keywords	Frontotemporal dementia, GRN, Mutation, Parkinsonism, Progranulin
Persistent URL	doi.org/10.1016/j.parkreldis.2010.05.001, hdl.handle.net/1765/20373
Journal	Parkinsonism & Related Disorders
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Di Fabio, R., Tessa, A., Simons, E., Santorelli, F., Casali, C., Serrao, M., Pierelli, F.& Bonifati, V. (2010). Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation. Parkinsonism & Related Disorders, 16(7), 484–485.https://doi.org/10.1016/j.parkreldis.2010.05.001

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