FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

Accumulation of the DNA/RNA binding protein fused in sarcoma as cytoplasmic inclusions in neurons and glial cells is the pathological hallmark of all patients with amyotrophic lateral sclerosis with mutations in FUS as well as in several subtypes of frontotemporal lobar degeneration, which are not a...

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Main Authors: Neumann, Manuela, Bentmann, Eva, Dormann, Dorothee, Jawaid, Ali, DeJesus-Hernandez, Mariely, Ansorge, Olaf, Roeber, Sigrun, Kretzschmar, Hans A., Munoz, David G., Kusaka, Hirofumi, Yokota, Osamu, Ang, Lee-Cyn, Bilbao, Juan, Rademakers, Rosa, Haass, Christian, Mackenzie, Ian R. A.
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2011
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Original Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3170539/
https://ncbi.nlm.nih.gov/pubmed/21856723
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awr201
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