A novel mutation of IL1RN in the deficiency of interleukin-1 receptor antagonist syndrome: Description of two unrelated cases from Brazil-Reference-Cited by-同舟云学术

A novel mutation of IL1RN in the deficiency of interleukin-1 receptor antagonist syndrome: Description of two unrelated cases from Brazil

Published:2011-11-29 Issue:12 Volume:63 Page:4007-4017
ISSN:0004-3591
Container-title:Arthritis & Rheumatism
language:en
Short-container-title:Arthritis & Rheumatism

Author:

Jesus Adriana A.,Osman Mazen,Silva Clovis A.,Kim Peter W.,Pham Tuyet-Hang,Gadina Massimo,Yang Barbara,Bertola Débora R.,Carneiro-Sampaio Magda,Ferguson Polly J.,Renshaw Blair R.,Schooley Ken,Brown Michael,Al-Dosari Asma,Al-Alami Jamil,Sims John E.,Goldbach-Mansky Raphaela,El-Shanti Hatem

Publisher

Wiley

Subject

Pharmacology (medical),Immunology,Rheumatology,Immunology and Allergy

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4. Phenotype-genotype analysis of cryopyrin-associated periodic syndromes (CAPS): description of a rare non-exon 3 and a novel CIAS1 missense mutation;Jesus;J Clin Immunol,2008

5. De novo CIAS1 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;Aksentijevich;Arthritis Rheum,2002

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