Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia

OBJECTIVE: Mutations in profilin-1 (PFN1) have recently been identified in patients with amyotrophic lateral sclerosis (ALS). Because of the considerable overlap between ALS and the common subtype of frontotemporal dementia, which is characterized by transactive response DNA-binding protein 43 patho...

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Detalhes bibliográficos
Main Authors: van Blitterswijk, Marka, Baker, Matthew C., Bieniek, Kevin F., Knopman, David S., Josephs, Keith A., Boeve, Bradley, Caselli, Richard, Wszolek, Zbigniew K., Petersen, Ronald, Graff-Radford, Neill R., Boylan, Kevin B., Dickson, Dennis W., Rademakers, Rosa
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3923463/
https://ncbi.nlm.nih.gov/pubmed/23634771
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/21678421.2013.787630
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