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Published in 2019 at "Cell reports"
DOI: 10.1016/j.celrep.2019.05.006
Abstract: Loss-of-function mutations in CNTNAP2 cause a syndromic form of autism spectrum disorder in humans and produce social deficits, repetitive behaviors, and seizures in mice. However, the functional effects of these mutations at cellular and circuit…
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Keywords:
prefrontal synaptic;
autism;
synaptic connectivity;
reduced prefrontal ... See more keywords