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注意：仅列出部分参考文献，下载原文获取全部文献信息。Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses
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Reversal of neurological defects in a mouse model of Rett syndrome
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Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
AL Collins et al.
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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
MD Shahbazian et al.
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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
J Guy et al.
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