| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6280230 | Neuroscience Letters | 2016 | 4 Pages |
Abstract
Even though these results suggest that the studied mutations are quite rare in SPD patients, the most frequent L444P mutation of the GBA gene may be associated with the development of EOPD in the Hungarian population.
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Life Sciences
Neuroscience
Neuroscience (General)
Authors
Rita Török, Dénes Zádori, Nóra Török, Ãva Csility, László Vécsei, Péter Klivényi,