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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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Bibliografiske detaljer
Udgivet i:PLoS One
Main Authors: 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
Sprog:Inglês
Udgivet: Public Library of Science 2016
Fag:
Online adgang: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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