Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of theCIAS1 gene and response to interleukin-1 receptor antagonist treatment-Reference-Cited by-同舟云学术

Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of theCIAS1 gene and response to interleukin-1 receptor antagonist treatment

Published:2006-04-15 Issue:8 Volume:140A Page:883-886
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Boschan C.,Witt O.,Lohse P.,Foeldvari I.,Zappel H.,Schweigerer L.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. 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

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

3. Neonatal Onset Multisystem Inflammatory Disease

4. Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra

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

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