AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). (Q37585836)

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scientific article published on 12 June 2013
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AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome).
scientific article published on 12 June 2013

    Statements

    AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). (English)
    Pierre Cacciagli
    Nadine Girard
    Laurent Villard
    12 June 2013
    363-368

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