A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency (Q36358469)

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A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency
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    A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency (English)
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    Qing Zhou
    Jillian Brady
    Afzal Sheikh
    Debra A Long Priel
    Deborah Stone
    Javed Khan
    20 September 2012
    713-720

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