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Patients with sporadic FTLD exhibit similar increases in lysosomal proteins and storage material as patients with FTD due to GRN mutations
Document Type
Article
Author
Davis, S.E.; Cook, A.K.; Hall, J.A.; Voskobiynyk, Y.; Boyle, N.R.; Hakim, A.R.; Anderson, K.M.; Hobdy, K.P.; Pugh, D.A.; Murchison, C.F.; Simmons, M.; Cowell, R.M.; Arrant, A.E.; Carullo, N.V.; McMeekin, L.J.; Margolies, K.A.; Nana, A.L.; Spina, S.; Grinberg, L.T.; Miller, B.L.; Seeley, W.W.
Source
In: Acta Neuropathologica Communications. (Acta Neuropathologica Communications, December 2023, 11(1))
Subject
Language
English
ISSN
20515960

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