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[期刊论文] 作者：Zi-Xian Yu,Dan-Yang Wang,Xiao-Hong Xu,
来源：神经科学通报（英文版） 年份：2020
Methyl-CpG-binding protein 2 (MeCP2) is broadly recognized as the genetic cause of Rett Syndrome (RTT), a devastating neurodevelopmental disorder with the progressive loss in motor skills and speech that is found almost exclusively in young......
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