Ontology highlight
ABSTRACT:
SUBMITTER: Kerr B
PROVIDER: S-EPMC2902516 | biostudies-literature | 2010
REPOSITORIES: biostudies-literature
Kerr Bredford B Silva Pamela A PA Walz Katherina K Young Juan I JI
PloS one 20100712 7
<h4>Background</h4>Rett syndrome (RTT) is an X-linked postnatal neurodevelopmental disorder caused by mutations in the gene encoding methyl-CpG binding protein 2 (MeCP2) and one of the leading causes of mental retardation in females. RTT is characterized by psychomotor retardation, purposeless hand movements, autistic-like behavior and abnormal gait. We studied the effects of environmental enrichment (EE) on the phenotypic manifestations of a RTT mouse model that lacks MeCP2 (Mecp2(-/y)).<h4>Pri ...[more]