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The Role of Glucocerebrosidase Mutations in Parkinson Disease and Lewy Body Disorders
Mutations in the gene encoding glucocerebrosidase (GBA), the enzyme deficient in the lysosomal storage disorder Gaucher disease, are associated with the development of Parkinson disease and other Lewy body disorders. In fact, GBA variants are currently the most common genetic risk factor associated...
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| Main Authors: | , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2010
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3529411/ https://ncbi.nlm.nih.gov/pubmed/20425034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11910-010-0102-x |
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