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Mutational analysis of TARDBP in Parkinson's disease

Authors :
van Blitterswijk, Marka
van Es, Michael A.
Verbaan, Dagmar
van Hilten, Jacobus J.
Scheffer, Hans
van de Warrenburg, Bart P.
Veldink, Jan H.
van den Berg, Leonard H.
Source :
Neurobiology of Aging. May2013, Vol. 34 Issue 5, p1517.e1-1517.e3. 0p.
Publication Year :
2013

Abstract

Abstract: Mutations in TAR DNA-binding protein (TARDBP) are associated with heterogenic phenotypes, including amyotrophic lateral sclerosis, frontotemporal dementia, and Parkinson''s disease. In this study, we investigated the presence of TARDBP mutations in a cohort of 429 Dutch patients with Parkinson''s disease. Though we detected 1 silent mutation, p.S332S, no missense mutations were present in our cohort. Our findings, therefore, demonstrate that TARDBP mutations do not appear to contribute to the pathogenesis of Parkinson''s disease in The Netherlands. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01974580
Volume :
34
Issue :
5
Database :
Academic Search Index
Journal :
Neurobiology of Aging
Publication Type :
Academic Journal
Accession number :
85395538
Full Text :
https://doi.org/10.1016/j.neurobiolaging.2012.09.013