Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation

2017-08-01

Movement Disorders , Volume 32 - Issue 8 p. 1259- 1260

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Keywords	ceroid lipofuscinosis inclusions, corticobasal syndrome, frontotemporal lobar degeneration, granulin gene, lysosomal storage
Persistent URL	doi.org/10.1002/mds.27049, hdl.handle.net/1765/108515
Journal	Movement Disorders
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA 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	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

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