Phospholipase C-gamma 2 activity in familial steroid-sensitive nephrotic syndrome

Genetics of childhood steroid-sensitive nephrotic syndrome

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Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

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Familial steroid-sensitive idiopathic nephrotic syndrome: seven cases from three families in China

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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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The B cell receptor-induced calcium flux involves a calcium mediated positive feedback loop

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Cold Urticaria, Immunodeficiency, and Autoimmunity Related toPLCG2Deletions

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

Phospholipase Cγ-2 and Intracellular Calcium Are Required for Lipopolysaccharide-induced Toll-like Receptor 4 (TLR4) Endocytosis and Interferon Regulatory Factor 3 (IRF3) Activation

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

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