The Ups and Downs of BDNF in Rett Syndrome

Abstract

Rett syndrome (RTT) is an X-linked postnatal neurodevelopmental disorder, which is primarily caused by mutations in the gene encoding methyl-CpG binding protein 2 (MeCP2). A number of MeCP2 target genes have been identified, including the neurotrophic factor BDNF; however, the functional relevance of these targets has not been established. In this issue of… (More)
DOI: 10.1016/j.neuron.2006.01.014

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