Ontology highlight
ABSTRACT:
SUBMITTER: Yue Y
PROVIDER: S-EPMC8535852 | biostudies-literature | 2021 Oct
REPOSITORIES: biostudies-literature

Science advances 20211022 43
Rett syndrome (RTT) is a severe neurodevelopmental disorder caused by loss of function of the X-linked methyl-CpG–binding protein 2 (<i>MECP2</i>). Several case studies report that gross motor function can be improved in children with RTT through treadmill walking, but whether the MeCP2-deficient motor circuit can support actual motor learning remains unclear. We used two-photon calcium imaging to simultaneously observe layer (L) 2/3 and L5a excitatory neuronal activity in the motor cortex (M1) ...[more]