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TARDBP mutations in Parkinson's disease.
by:
Sruti Rayaprolu ,
Shinsuke Fujioka ,
Sharleen Traynor ,
Alexandra I. Soto-Ortolaza ,
Leonard Petrucelli ,
Dennis W. Dickson ,
Rosa Rademakers ,
Kevin B. Boylan ,
Neill R. Graff-Radford ,
Ryan J. Uitti ,
Zbigniew K. Wszolek ,
Owen A. Ross
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Abstract
Mutations of the TARDBP gene encoding TDP-43 protein have been shown to cause amyotrophic lateral sclerosis and have been reported to present with clinical heterogeneity including parkinsonism. In addition, TDP-43 pathology has been observed across a spectrum of neurodegenerative disorders, including Alzheimer's and Parkinson's disease. Herein we report the presence of a TDP-43 mutation in a patient with a clinical diagnosis of Parkinson's disease. The TDP-43 p.N267S substitution has been previously implicated in both amyotrophic lateral sclerosis and behavioral variant frontotemporal dementia. Our findings widen the phenotypic presentation for the TDP-43 p.N267S substitution and support a possible role for rare TDP-43 mutations presenting with Parkinson's disease. Copyright © 2012 Elsevier Ltd. All rights reserved.
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