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Medical News Article on Research
Selective deletion of Rett syndrome gene provides insight into origin of complex behaviors
2008 OCT 6 -- A new study describes an exciting approach for mapping the specific neuronal origins of complex and varied behaviors characteristic of Rett syndrome (RTT), an autism spectrum disorder. The research, published by Cell Press in the September 25th issue of the journal Neuron, also uncovers a novel and unexpected role for the gene that causes RTT.
RTT is a devastating neurological disorder associated with a broad array of abnormalities that impact almost every part of the nervous system. The majority of RTT cases are caused by mutations in the methyl-CpG-binding protein (MECP2) gene, which encodes MeCP2, a protein widely expressed...
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