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112 MeCP2 deletions or point mutations on the X chromosome in females manifest as Rett syndrome, a serious neurological disorder with autism-like symptoms

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hyperemia/hemorrhage was graded from focal to diffuse according to lamina propria or subendothelial localization

10.1186/s10020-021-00307-1 135 YangN.GuanQ.-W.ChenF.-H.XiaQ.-X.YinX.-X.ZhouH.-H.et al (2020)