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The association between ß-glucocerebrosidase mutations and parkinsonism
Mutations in the ß-glucocerebrosidase gene (GBA), which encodes the lysosomal enzyme ß-glucocerebrosidase, have traditionally been implicated in Gaucher disease, an autosomal-recessive lyososomal storage disorder. Yet the past two decades have yielded an explosion of epidemiological and basic-scienc...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3816495/ https://ncbi.nlm.nih.gov/pubmed/23812893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11910-013-0368-x |
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