Cryopyrin-Associated Periodic Syndrome
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2012.01812.x/fullpdf
Reference17 articles.
1. New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes;Dodé;Am J Hum Genet,2002
2. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome;Hoffman;Nat Genet,2001
3. The emerging role of interleukin-1β in autoinflammatory diseases;Lachmann;Arthritis Rheum,2011
4. Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes;Feldmann;Am J Hum Genet,2002
5. Neurological manifestations of the Mendelian-inherited autoinflammatory syndromes;Montealegre Sanchez;Dev Med Child Neurol,2009
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