| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5502510 | Journal of the Neurological Sciences | 2017 | 5 Pages |
Abstract
Our results suggest that specific mutations in GBA and LRRK2 influence the clinical signs of the disease, with significant implications for handling of specific patient groups.
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Authors
Camilla P. da Silva, Gabriella de M. Abreu, Pedro H. Cabello Acero, Mário Júnior, João S. Pereira, Sarah R. de A. Ramos, Caroline M. Nascimento, Danielle D. Voigt, Ana Lucia Rosso, Marco A. Araujo Leite, Luiz Felipe R. Vasconcellos,