Association of mannose binding lectin codon 54 polymorphism with predisposition to Henoch-Schönlein purpura in childhood
Author:
Affiliation:
1. Department of Medical Genetics; Faculty of Medicine; Ege University; Izmir Turkey
2. Department of Pediatrics; Behcet Uz Children's Hospital; Izmir Turkey
Publisher
Wiley
Subject
Rheumatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/1756-185X.12321/fullpdf
Reference20 articles.
1. Pulmonary hemorrhage associated with henoch-schönlein purpura in pediatric patients: case report and review of the literature;Chen;Semin Arthritis Rheum,2011
2. Henoch-Schönlein purpura in children report of 100 patients and review of the literature;Saulsbury;Medicine,1999
3. Henoch-Schönlein purpura;Saulsbury;Curr Opin Rheumatol,2001
4. Relationship between gene polymorphisms of mannose-binding lectin (MBL) and two molecular forms of MBL;Terai;Eur J Immunol,2003
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1. Lack of Association Between HMGB1 Gene Polymorphism and Risk of Henoch–Schönlein Purpura in Childhood;Iranian Journal of Pediatrics;2022-04-01
2. Genetics of immunoglobulin-A vasculitis (Henoch-Schönlein purpura): An updated review;Autoimmunity Reviews;2018-03
3. Mannose-binding lectin (MBL) codon 54 (rs1800450) polymorphism predisposes towards medium vessel vasculitis in patients with systemic lupus erythematosus;Clinical Rheumatology;2017-01-17
4. Genetics of vasculitis;Current Opinion in Rheumatology;2015-01
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