Cytochrome oxidase mutations aiding diagnosis of sporadic alzheimer's disease
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机译：细胞色素氧化酶突变有助于诊断偶发性阿尔茨海默氏病
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摘要
The present invention relates to genetic mutations in mitochondrial cytochrome oxidase genes that segregate with Alzheimer's disease (AD). The invention provides methods for detecting such mutations, as a diagnostic for Alzheimer's Disease, either before or after the onset clinical symptoms. The invention further provides treatment of cytochrome oxidase dysfunction.
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