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Saxby, P.T

TC: Conceptualization, Writing review & editing

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

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

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