A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency (Q36358469)
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English | 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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Susan Moir
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Ivona Aksentijevich
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Daniel L Kastner
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Marta S Martins
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Amanda Ombrello
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Joshua D Milner
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Geun-Shik Lee
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Shrimati Datta
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Tom D Bunney
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Matilda Katan
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Douglas B Kuhns
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Qing Zhou
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Jillian Brady
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Afzal Sheikh
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Debra A Long Priel
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Deborah Stone
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Javed Khan
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20 September 2012
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Identifiers
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