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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2013
Matèries:
Article
Accés en línia: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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