Genetics
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-540-75387-2_6
Reference63 articles.
1. Aganna E, Martinon F, Hawkins PN et al (2002) Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis. Arthritis Rheum 46(9):2445–2452
2. Ahmad T, Wallace GR, James T et al (2003) Mapping the HLA association in Behcet’s disease: a role for tumor necrosis factor polymorphisms? Arthritis Rheum 48(3):807–813
3. Akman A, Sallakci N, Coskun M et al (2006) TNF-alpha gene 1031 T/C polymorphism in Turkish patients with Behcet’s disease. Br J Dermatol 155(2):350–356
4. Aksentijevich I, Nowak M, Mallah M et al (2002) 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. Arthritis Rheum 46(12):3340–3348
5. Alayli G, Aydin F, Coban AY et al (2007) T helper 1 type cytokines polymorphisms: association with susceptibility to Behcet’s disease. Clin Rheumatol 26(8):1299–1305
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