The Ups and Downs of BDNF in Rett Syndrome

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The Ups and Downs of BDNF in Rett Syndrome

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 Neuron, Chang et al. provide the first...

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ژورنال

عنوان ژورنال: Neuron

سال: 2006

ISSN: 0896-6273

DOI: 10.1016/j.neuron.2006.01.014