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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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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Korean Neurological Association
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3131546/ https://ncbi.nlm.nih.gov/pubmed/21779299 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2011.7.2.99 |
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