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Thromb Haemost 2004; 91(04): 830-831
DOI: 10.1055/s-0037-1614275
DOI: 10.1055/s-0037-1614275
Letters to the Editor
A nucleic acid exchange in Intron F (Intron F-14T>G) in the human plasminogen gene is only a common polymorphism and not a true mutation
Further Information
Publication History
Received
12 August 2003
Accepted after revision
05 November 2003
Publication Date:
08 December 2017 (online)
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References
- 1 Sartori MT, Saggiorato G, Pellati D. et al.. Contraceptive pills induce an improvement in congenital hypoplasminogenemia in two unrelated patients with ligneous conjunctivitis. Thromb Haemost 2003; 90: 86-91.
- 2 Schuster V, Seregard S. Ligneous conjunctivitis. Surv Ophthalmol 2003; 48: 369-88.
- 3 Tefs K, Tail RC, Walker ID. et al.. A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenemia. Blood Coagul Fibrinolysis 2003; 14: 411-6.
- 4 Schuster V, Seidenspinner S, Zeitler P. et al.. Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis. Blood 1999; 93: 3457-66.
- 5 Schuster V, Zeitler P, Seregard S. et al.. Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis. Thromb Haemost 2001; 85: 1004-10.