TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

BACKGROUND: TDP-43 is a major component of the ubiquitinated inclusions that characterise amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) with ubiquitin inclusions (FTLD-U). TDP-43 is an RNA-binding and DNA-binding protein that has many functions and is encoded by th...

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Main Authors: Van Deerlin, Vivianna M., Leverenz, James B., Bekris, Lynn M., Bird, Thomas D., Yuan, Wuxing, Elman, Lauren B., Clay, Dana, Wood, Elisabeth McCarty, Chen-Plotkin, Alice S., Martinez-Lage, Maria, Steinbart, Ellen, McCluskey, Leo, Grossman, Murray, Neumann, Manuela, Wu, I-Lin, Yang, Wei-Shiung, Kalb, Robert, Galasko, Douglas R., Montine, Thomas J., Trojanowski, John Q., Lee, Virginia M.-Y., Schellenberg, Gerard D., Yu, Chang-En
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3546119/
https://ncbi.nlm.nih.gov/pubmed/18396105
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1474-4422(08)70071-1
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