Additional Metadata
Keywords ceroid lipofuscinosis inclusions, corticobasal syndrome, frontotemporal lobar degeneration, granulin gene, lysosomal storage
Persistent URL dx.doi.org/10.1002/mds.27049, hdl.handle.net/1765/108515
Journal Movement Disorders
Citation
Terlizzi, R. (Rossana), Valentino, M.L, Bartoletti-Stella, A. (Anna), Columbaro, M. (Marta), Piras, S. (Silvia), Stanzani-Maserati, M. (Michelangelo), … Capellari, S. (2017). Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation. Movement Disorders, 32(8), 1259–1260. doi:10.1002/mds.27049