Association of a Mutation inLACC1With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis

Author:

Wakil Salma M.1,Monies Dorota M.1,Abouelhoda Mohamed1,Al-Tassan Nada1,Al-Dusery Haya2,Naim Ewa A.1,Al-Younes Banan1,Shinwari Jameela2,Al-Mohanna Futwan A.2,Meyer Brian F.1,Al-Mayouf Sulaiman2

Affiliation:

1. King Faisal Specialist Hospital and Research Centre, and King Abdulaziz City for Science and Technology; Riyadh Saudi Arabia

2. King Faisal Specialist Hospital and Research Centre; Riyadh Saudi Arabia

Funder

King Faisal Specialist Hospital & Research Centre, Riyadh

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

Reference44 articles.

1. International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001;Petty;J Rheumatol,2004

2. Clinical analysis of 570 cases with juvenile rheumatoid arthritis: results of a nationwide retrospective survey in Japan;Fujikawa;Acta Paediatr Jpn,1997

3. Paediatric rheumatology: a global perspective;Sawhney;Best Pract Res Clin Rheumatol,2006

4. The diagnostic significance of soluble CD163 and soluble interleukin-2 receptor α-chain in macrophage activation syndrome and untreated new-onset systemic juvenile idiopathic arthritis;Bleesing;Arthritis Rheum,2007

5. Novel IL10 gene family associations with systemic juvenile idiopathic arthritis;Fife;Arthritis Res Ther,2006

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