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Molecular and Cellular Phenotypes of AUTS2 Deficiency in the Developing Mouse Cortex and Hippocampus
Variants in the gene Autism Susceptibility Candidate 2 (AUTS2) are a rare cause of intellectual disability, developmental delay and autistic features in patients. However, the mechanism by which loss of AUTS2 causes specific neurological symptoms, the underlying neuroanatomical abnormalities, and the syndrome’s pathological ...