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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: Ramsey, Chenere P., Giasson, Benoit I.
格式: Artigo
語言:Inglês
出版: 2008
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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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