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AChR胸腺中异位表达异常导致MG发病的研究 被引量:2

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摘要 重症肌无力(myasthenia gravis,MG)是一种自身免疫性疾病,由抗体介导,主要攻击神经肌肉接头处的乙酰胆碱受体,引起全身骨骼肌无力和易疲劳。经研究分析,胸腺内的免疫耐受异常在发病机制中占重要作用,本研究将讨论在重症肌无力发病中胸腺内的自身免疫反应以及编码乙酰胆碱自身抗原α亚基的基因——CHRNAl基因位点多态性在重症肌无力发病机制中的相关作用。
作者 王田 张莹
出处 《卒中与神经疾病》 2015年第4期253-255,共3页 Stroke and Nervous Diseases
基金 哈尔滨市科技创新人才研究专项资金项目(青年后备人才)资助编号为(2014RFQGJ006)
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二级参考文献1

  • 1J?rn P. Sieb,Simone Kraner,Michael Rauch,Ortrud K. Steinlein. Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by ε-AChR subunit truncating mutations[J] 2000,Human Genetics(2):160~164

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