The expression of methyl CpG binding fac
โ
Jung, Benjamin P. ;Jugloff, Denis G.M. ;Zhang, Guangming ;Logan, Richard ;Brown,
๐
Article
๐
2003
๐
John Wiley and Sons
๐
English
โ 382 KB
## Abstract Mutations in the MeCP2 gene cause Rett syndrome, a neurologic condition affecting primarily young girls. To gain insight into the normal function of MeCP2, we examined its temporal and spatial expression patterns, and immunoreactive prevalence, during late embryonic and perinatal brain