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Duchenne型肌营养不良肌肉病变机制研究 被引量:3

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摘要 Duchenne型肌营养不良(DMD)是一种X连锁隐性遗传的致死性肌病,至今尚无有效治疗方法,尽管人类对DMD致病基因及其产物抗肌萎缩蛋白的研究已有15年之久,然而对抗肌萎缩蛋白缺失如何引起肌肉变性、坏死的具体机制至今仍不清楚,因此有必要对DMD发病机制做进一步研究。目前对DMD的发病机制主要有两种假说,一种是机械损伤假说,另一种是钙稳态失衡假说。
出处 《中国神经免疫学和神经病学杂志》 CAS 2008年第2期141-143,共3页 Chinese Journal of Neuroimmunology and Neurology
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