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A Hypermorphic Missense Mutation in PLCG2, Encoding Phospholipase Cγ2, Causes a Dominantly Inherited Autoinflammatory Disease with Immunodeficiency

Author:

Qing Zhou,Geun-Shik Lee,Jillian Brady,Shrimati Datta,Matilda Katan,Afzal Sheikh,Marta S. Martins,Tom D. Bunney,Brian H. Santich,Susan Moir,Douglas B. Kuhns,Debra A. Long Priel,Amanda Ombrello,Deborah Stone,Michael J. Ombrello,Javed Khan et al.

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

5 October 2012

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