Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome
Rett syndrome (RTT) arises from loss-of-function mutations in methyl-CpG binding protein 2 gene (Mecp2), but fundamental aspects of its physiological mechanisms are unresolved. Here, by whole-cell recording of synaptic responses in MeCP2 mutant mice in vivo, we show that visually driven excitatory a...
Main Authors: | , , , , , , , , , |
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Format: | Article |
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National Academy of Sciences (U.S.)
2018
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Online Access: | http://hdl.handle.net/1721.1/114900 https://orcid.org/0000-0003-2011-2897 https://orcid.org/0000-0002-1701-325X https://orcid.org/0000-0002-0737-2558 https://orcid.org/0000-0003-2442-5671 |