Article

Hippocampal circuit abnormalities in MeCP2+/- mouse model of Rett syndrome

2015-12-18

Abstract excerpt

Rett syndrome (RTT) has a complex developmental course over childhood and adolescence. Patients with RTT often have a pre-symptomatic period with no or little outward signs of the disorder, followed by developmental arrest and regression. Following regression, the individual's condition is not static, as they often progress into defined stages with unique neurological symptoms. Similarly, the progression of RTT-li...

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Literature Corpus work: af31def8-2a27-55ff-80a8-1e02a5b235e9
DOI: 10.1101/034835

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