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
Language Label Description Also known as
English
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

    title
    AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). (English)
    1 reference
    stated in
    Europe PubMed Central
    PMC publication ID
    3925263
    retrieved
    21 August 2017
    main subject
    disability
    0 references
    cites work

    Identifiers

     
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