Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid

Published 2013 View Full Article

Title

Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid

Authors

Keywords

Amyotrophic Lateral Sclerosis, Sporadic Amyotrophic Lateral Sclerosis, Neuronal Cytoplasmic Inclusion, C9orf72 Mutation, Basophilic Inclusion Body Disease

Journal

ACTA NEUROPATHOLOGICA

Volume 125, Issue 3, Pages 463-465

Publisher

Springer Nature

Online

2013-02-02

DOI

10.1007/s00401-013-1089-6

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