RettSyndrome相关论文
...
Rett syndrome (RTT) is a severe neurodevelopmental disorder.Recently,mutations in X-linked cyclin-dependent kinase-like ......
The methyl-CpG-binding protein 2(MeCP2)gene,MECP2,is an X-linked gene encoding the MeCP2 protein and mutations of MECP2 ......
MeCP2 reinforces STAT3 signaling and effector T cell differentiation by controlling miR-124 mediated
...
Rett syndrome (RTT) is a progressive neurodevelop-mental disorder,mainly caused by mutations in MeCP2 and currently with......
Rett syndrome(RTT)is a progressive neurological disorder caused by mutations in the X-linked gene methyl-CpG-binding......
