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Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
Mutations in the glucocerebrosidase gene (GBA), which cause Gaucher disease, are also potent risk factors for Parkinson’s disease. We examined whether a genetic burden of variants in other lysosomal storage disorder genes is more broadly associated with Parkinson’s disease susceptibility. The sequen...
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| 出版年: | Brain |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5841393/ https://ncbi.nlm.nih.gov/pubmed/29140481 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awx285 |
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