Additional Metadata
Keywords Frontotemporal dementia, GRN, Mutation, Parkinsonism, Progranulin
Persistent URL dx.doi.org/10.1016/j.parkreldis.2010.05.001, hdl.handle.net/1765/20373
Citation
Di Fabio, R, Tessa, A, Simons, E.J, Santorelli, F.M, Casali, C, Serrao, M, … Bonifati, V. (2010). Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation. Parkinsonism & Related Disorders, 16(7), 484–485. doi:10.1016/j.parkreldis.2010.05.001