PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes

Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated WithPLCG2Mutations

(2015) Oyinade M. Aderibigbe et al.   JAMA Dermatology

The autoinhibitory C-terminal SH2 domain of phospholipase C- 2 stabilizes B cell receptor signalosome assembly

(2014) J. Wang et al.   Science Signaling

Urticaria mimickers in children

(2013) Anubhav N. Mathur et al.   Dermatologic Therapy

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

(2012) Qing Zhou et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Physical Urticaria

(2012) Marina Abajian et al.   CURRENT ALLERGY AND ASTHMA REPORTS

Cold Urticaria, Immunodeficiency, and Autoimmunity Related toPLCG2Deletions

(2012) Michael J. Ombrello et al.   NEW ENGLAND JOURNAL OF MEDICINE

Structural and Functional Integration of the PLCγ Interaction Domains Critical for Regulatory Mechanisms and Signaling Deregulation

(2012) Tom D. Bunney et al.   STRUCTURE

A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model

(2011) Koichiro Abe et al.   ARTHRITIS AND RHEUMATISM

Familial atypical cold urticaria: Description of a new hereditary disease

(2009) Chhavi Gandhi et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY