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Thromb Haemost 2001; 86(02): 716-717
DOI: 10.1055/s-0037-1616112
DOI: 10.1055/s-0037-1616112
Letters to the Editor
A New Mutation Trans to I278T Cystathionine β-synthase Associated with Factor V Leiden Causes Mild Homocystinuria but Severe Vascular Disease
Further Information
Publication History
Received
28 December 2000
Accepted after resubmission
12 March 2001
Publication Date:
12 December 2017 (online)
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References
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- 4 Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, van Der Velden PA, Reitsma P. Mutation in blood coagulation factor V associated with resistance to activated Protein C. Nature 1994; 369: 64-7.
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- 7 Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, Fowler B, Seligsohn U. Coexistance of hereditary homocystinuria and factor V Leiden effect on thrombosis. N Engl J Med 1996; 334: 753.
- 8 Kraus JP, Janosik M, Kozich V, Mandell R, Shih V, Sperandeo MP, Sebastio G, De Franchis R. et al. Cystathionine β-synthase mutations in homocystinuria. Human Mutation 1999; 13: 362-75.