| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10745748 | Parkinsonism & Related Disorders | 2013 | 4 Pages |
Abstract
Larger population based studies are needed to determine the pathogenicity of the A18T and A29S substitutions. Our findings highlight the possible role of rare variants contributing to disease risk and may support further screening of the SNCA gene in sporadic PD patients from different populations.
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Authors
Dorota Hoffman-Zacharska, Dariusz Koziorowski, Owen A. Ross, MichaÅ Milewski, JarosÅaw PoznaÅski, Marta Jurek, Zbigniew K. Wszolek, Alexandra Soto-Ortolaza, JarosÅaw SÅawek, Piotr Janik, Zygmunt Jamrozik, Anna Potulska-Chromik,