GBA Variants Influence Motor and Non-Motor Features of Parkinson’s Disease

The presence of mutations in glucocerebrosidase (GBA) gene is a known factor increasing the risk of developing Parkinson’s disease (PD). Mutations carriers have earlier disease onset and are more likely to develop neuropsychiatric symptoms than other sporadic PD cases. These symptoms have primarily...

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Publicat a:PLoS One
Autors principals: Jesús, Silvia, Huertas, Ismael, Bernal-Bernal, Inmaculada, Bonilla-Toribio, Marta, Cáceres-Redondo, María Teresa, Vargas-González, Laura, Gómez-Llamas, Myriam, Carrillo, Fátima, Calderón, Enrique, Carballo, Manuel, Gómez-Garre, Pilar, Mir, Pablo
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2016
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5193380/
https://ncbi.nlm.nih.gov/pubmed/28030538
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0167749
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