Methylenetetrahydrofolate reductase C677T polymorphism in patients with Henoch-Schönlein purpura
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2010.03247.x/fullpdf
Reference28 articles.
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2. Methylentetrahydrofolate reductase polymorphism in Kawasaki disease;Tsukahara;Pediatr. Int.,2000
3. Common C677T polymorphism of the methylentetra hydrofolate reductase gene and the risk of venous tromboembolism: Meta analysis of 31 studies;Ray;Pathophysiol. Haemost. Tromb.,2002
4. A case control study on the contribution of factor V-leiden, prothrombin G 20210A and MTHFR C677T mutations to the genetic susceptibility of deep venous trombosis;Almawı;J. Thromb. Thrombolysis,2005
5. MTHFR association with arteriosclerotic vascular disease?;Fletcher;Hum. Genet.,1998
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1. Predictive biomarkers of IgA vasculitis with nephritis by metabolomic analysis;Seminars in Arthritis and Rheumatism;2020-12
2. Genetics of immunoglobulin-A vasculitis (Henoch-Schönlein purpura): An updated review;Autoimmunity Reviews;2018-03
3. The genetics of Henoch–Schönlein purpura: a systematic review and meta-analysis;Rheumatology International;2013-01-17
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