Altered morphology of YFP-expressing neurons in a Rett Syndrome mouse model
Rett Syndrome (RTT, OMIM 312750) is a pervasive autism spectrum disorder affecting 1 in 10,000 females. The majority of cases are caused by mutations in the X-linked gene MECP2. The RTT phenotype appears to be caused by impaired synapse maturation or maintenance, resulting in disrupted autonomic...
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| Language: | English en |
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2010
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| Online Access: | http://hdl.handle.net/1828/3119 |