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Visual short-term memory deficits associated with GBA mutation and Parkinson’s disease

Individuals with mutation in the lysosomal enzyme glucocerebrosidase (GBA) gene are at significantly high risk of developing Parkinson’s disease with cognitive deficit. We examined whether visual short-term memory impairments, long associated with patients with Parkinson’s disease, are also present...

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Detalles Bibliográficos
Autores principales:	Zokaei, Nahid, McNeill, Alisdair, Proukakis, Christos, Beavan, Michelle, Jarman, Paul, Korlipara, Prasad, Hughes, Derralynn, Mehta, Atul, Hu, Michele T. M., Schapira, Anthony H. V., Husain, Masud
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2014
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107740/ https://www.ncbi.nlm.nih.gov/pubmed/24919969 http://dx.doi.org/10.1093/brain/awu143

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