| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8841641 | Neuroscience Letters | 2018 | 4 Pages |
Abstract
Our results confirm that the p. A53T SNCA mutation is relatively common in Greek patients with PD or PD plus dementia, particularly in cases with early onset and/or autosomal dominant family history.
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Authors
Marianthi Breza, Georgios Koutsis, Georgia Karadima, Constantin Potagas, Chrisoula Kartanou, Sokratis G. Papageorgiou, George P. Paraskevas, Elisabeth Kapaki, Leonidas Stefanis, Marios Panas,