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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:PLoS One
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Public Library of Science 2016
विषय:
Research Article
ऑनलाइन पहुंच: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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