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    Molecular and Cellular Phenotypes of AUTS2 Deficiency in the Developing Mouse Cortex and Hippocampus 

    Castanza, Anthony Scott
    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 ...

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    Author
    Castanza, Anthony Scott (1)
    SubjectAutism (1)AUTS2 (1)Dentate Gyrus (1)Developmental biology (1)Intellectual Disability (1)
    Molecular biology (1)
    Neocortex (1)
    Neurodevelopment (1)
    Neurosciences (1)
    Pathology (1)
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