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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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| Vydáno v: | Brain |
|---|---|
| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2017
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| Témata: | |
| On-line přístup: | 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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