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Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease.

Hoffman-Zacharska, Dorota and Koziorowski, Dariusz and Ross, Owen A and Milewski, Michał and Poznański, Jarosław and Jurek, Marta and Wszolek, Zbigniew K and Soto-Ortolaza, Alexandra and Sławek, Jarosław and Janik, Piotr and Jamrozik, Zygmunt and Potulska-Chromik, Anna and Jasińska-Myga, Barbara and Opala, Grzegorz and Krygowska-Wajs, Anna and Czyżewski, Krzysztof and Dickson, Dennis W and Bal, Jerzy and Friedman, Andrzej (2013) Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease. Parkinsonism & related disorders, 19 (11). pp. 1057-60. ISSN 1873-5126

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Abstract

Mutations in the α-synuclein-encoding gene SNCA are considered as a rare cause of Parkinson's disease (PD). Our objective was to examine the frequency of the SNCA point mutations among PD patients of Polish origin.

Item Type:Article
Subjects:R Medicine > R Medicine (General)
Divisions:Department of Biophysics
ID Code:632
Deposited By: Prof Jaroslaw Poznanski
Deposited On:18 Jun 2014 07:37
Last Modified:27 Oct 2014 14:02

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