A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency
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| Description | scientific article |
| Author/s |
author: Amanda K. Ombrello Matilda Katan Shrimati Datta Marta S. Martins Brian H Santich Ivona Aksentijevich Tom D Bunney Geun-Shik Lee Joshua D Milner Susan Moir Michael J. Ombrello Douglas B Kuhns Daniel L. Kastner |
| Publication date | September 20, 2012 |
| Language | English |
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