Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature-Reference-Cited by-同舟云学术

Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature

Published:2013 Issue:1 Volume:15 Page:R30
ISSN:1478-6354
Container-title:Arthritis Research & Therapy
language:en
Short-container-title:Arthritis Res Ther

Author:

Rowczenio Dorota M,Trojer Hadija,Russell Tonia,Baginska Anna,Lane Thirusha,Stewart Nicola M,Gillmore Julian D,Hawkins Philip N,Woo Patricia,Mikoluc Bozena,Lachmann Helen J

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy,Rheumatology

Reference38 articles.

1. The Inflammasome

2. De novoCIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin-associated autoinflammatory diseases

3. New Mutations of CIAS1 That Are Responsible for Muckle-Wells Syndrome and Familial Cold Urticaria: A Novel Mutation Underlies Both Syndromes

4. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndrome

5. Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes

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