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...

詳細記述

保存先:
書誌詳細
出版年:PLoS One
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2016
主題:
Research Article
オンライン･アクセス: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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