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The E163K DJ-1 Mutant Shows Specific Antioxidant Deficiency
Recent discoveries of genetic mutations linked to familial forms of Parkinson's disease (PD), including mutations in DJ-1, have provided insights into the pathogenesis of sporadic PD. Recently, a novel homozygous missense mutation in the gene encoding human DJ-1 protein resulting in the E163K a...
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| Main Authors: | , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2008
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2783860/ https://ncbi.nlm.nih.gov/pubmed/18822273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2008.09.009 |
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