Association of mutations in theNALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis-Reference-Cited by-同舟云学术

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Association of mutations in theNALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

Published:2002-09 Issue:9 Volume:46 Page:2445-2452
ISSN:0004-3591
Container-title:Arthritis & Rheumatism
language:en
Short-container-title:Arthritis & Rheumatism

Author:

Aganna Ebun,Martinon Fabio,Hawkins Philip N.,Ross John B.,Swan Daniel C.,Booth David R.,Lachmann Helen J.,Gaudet Roxanne,Woo Patricia,Feighery Conleth,Cotter Finbarr E.,Thome Margot,Hitman Graham A.,Tschopp J�rg,McDermott Michael F.

Publisher

Wiley

Subject

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

Reference26 articles.

1. Hereditary Periodic Fever

2. Hereditary periodic fever syndromes

3. TNFRSF1A mutations and autoinflammatory syndromes

4. Familial cold urticaria

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