Parkinsonism Associated with Glucocerebrosidase Mutation

BACKGROUND: Gaucher's disease is an autosomal recessive, lysosomal storage disease caused by mutations of the β-glucocerebrosidase gene (GBA). There is increasing evidence that GBA mutations are a genetic risk factor for the development of Parkinson's disease (PD). We report herein a famil...

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Detalles Bibliográficos
Autores principales: Sunwoo, Mun-Kyung, Kim, Seung-Min, Lee, Sarah, Lee, Phil Hyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131546/
https://www.ncbi.nlm.nih.gov/pubmed/21779299
http://dx.doi.org/10.3988/jcn.2011.7.2.99

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131546/
https://www.ncbi.nlm.nih.gov/pubmed/21779299
http://dx.doi.org/10.3988/jcn.2011.7.2.99

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