Glucocerebrosidase activity in Parkinson’s disease with and without GBA mutations

Glucocerebrosidase (GBA) mutations have been associated with Parkinson’s disease in numerous studies. However, it is unknown whether the increased risk of Parkinson’s disease in GBA carriers is due to a loss of glucocerebrosidase enzymatic activity. We measured glucocerebrosidase enzymatic activity...

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Vydáno v:Brain
Hlavní autoři: Alcalay, Roy N., Levy, Oren A., Waters, Cheryl C., Fahn, Stanley, Ford, Blair, Kuo, Sheng-Han, Mazzoni, Pietro, Pauciulo, Michael W., Nichols, William C., Gan-Or, Ziv, Rouleau, Guy A., Chung, Wendy K., Wolf, Pavlina, Oliva, Petra, Keutzer, Joan, Marder, Karen, Zhang, Xiaokui
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2015
Témata:
Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4564023/
https://ncbi.nlm.nih.gov/pubmed/26117366
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awv179
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