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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Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
Konular:
Article
Online Erişim: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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