Increased coupling of caveolin-1 and ERα contributes to the Fragile X syndrome

来源 :The 6th FAONS Congress and 11th Biennial Conference of CNS(第 | 被引量 : 0次 | 上传用户:lixiaobo59178
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  Objective: Fragile X syndrome(FXS)is a form of inherited mental retardation in humans that results from expansion of a CGG repeat in the Fmr1 gene.
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Mitochondria play critical role in neuronal function and survival and mitochondrial abnormalities and dysfunction have been well characterized in various neurodegenerative diseases including Alzheimer