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- W1499579683 abstract "17 Reddy LPM, Johansson M, Sturfelt G, Jonsen A, Gunnarsson I,Svenungsson E, Rantapaa-Dahlqvist S, Alarcon-Riquelme M. TheR620W C/T polymorphism of the gene PTPN22 is associated withSLE independently of the association of PDCD1. Genes Immun 2005;6: 658–62.18 Skorka A, Bednarczuk T, Bar-Andziak E, Nauman J, Ploski R.Lymphoidtyrosine phosphatase (PTPN22/LYP) variantandGraves sdisease in a Polish population: association and gene dose-dependentcorrelatation with the age of onset. Clin Endocrinol 2005; 62:679–82.19 Velaga M, Wilson V, Jennings C, Owens C, Herington S, DonaldsonP, Ball S, James R, Quinton R, Perros P, Pearce S. The codon 620tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene isamajordeterminantofGravesDisease. JClinEndocrinolMetab 2004;89: 5862–5." @default.
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- W1499579683 date "2010-09-01" @default.
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- W1499579683 title "Blood group significantly influences von Willebrand factor increase and half‐life after desmopressin in von Willebrand disease Vicenza" @default.
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- W1499579683 doi "https://doi.org/10.1111/j.1538-7836.2010.03957.x" @default.
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