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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מידע ביבליוגרפי
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
פורמט: Artigo
שפה:Inglês
יצא לאור: 2013
נושאים:
Article
גישה מקוונת: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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