| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10745045 | Parkinsonism & Related Disorders | 2015 | 6 Pages |
Abstract
The identification of this novel family contributes to the genetic and clinical characterization of this rare form. Our data reinforce the view that SNCA triplications cause early-onset parkinsonism, with prominent non-motor features.
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Authors
Simone Olgiati, Astrid Thomas, Marialuisa Quadri, Guido J. Breedveld, Josja Graafland, Hubertus Eussen, Hannie Douben, Annelies de Klein, Marco Onofrj, Vincenzo Bonifati,