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The risk of Parkinson's disease in type 1 Gaucher disease

In Gaucher disease, defective lysosomal glucocerebrosidase due to mutations in the GBA1 gene results in lysosomal accumulation of glucocerebroside in mononuclear phagocytes and a multisystemic phenotype. Observations of occurrence of Parkinson's disease in some patients with non-neuronopathic t...

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Detalhes bibliográficos
Main Authors: Bultron, Gilberto, Kacena, Katherine, Pearson, Daniel, Boxer, Michael, Yang, Ruhua, Sathe, Swati, Pastores, Gregory, Mistry, Pramod K.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2887303/
https://ncbi.nlm.nih.gov/pubmed/20177787
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-010-9055-0
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