A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

Neuronal intermediate filament inclusion disease and atypical frontotemporal lobar degeneration are rare diseases characterized by ubiquitin-positive inclusions lacking transactive response DNA-binding protein-43 and tau. Recently, mutations in the fused in sarcoma gene have been shown to cause fami...

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Detalhes bibliográficos
Main Authors: Lashley, Tammaryn, Rohrer, Jonathan D., Bandopadhyay, Rina, Fry, Charles, Ahmed, Zeshan, Isaacs, Adrian M., Brelstaff, Jack H., Borroni, Barbara, Warren, Jason D., Troakes, Claire, King, Andrew, Al-Saraj, Safa, Newcombe, Jia, Quinn, Niall, Ostergaard, Karen, Schrøder, Henrik Daa, Bojsen-Møller, Marie, Braendgaard, Hans, Fox, Nick C., Rossor, Martin N., Lees, Andrew J., Holton, Janice L., Revesz, Tamas
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3170529/
https://ncbi.nlm.nih.gov/pubmed/21752791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awr160
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