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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2014
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4107740/
https://ncbi.nlm.nih.gov/pubmed/24919969
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awu143
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