Thromb Haemost 2004; 91(04): 830-831
DOI: 10.1055/s-0037-1614275
Letters to the Editor
Schattauer GmbH

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

Katrin Tefs
,
Maike Ziegler
,
Maria Georgieva
,
Boris Hügle
,
Volker Schuster
Further Information

Publication History

Received 12 August 2003

Accepted after revision 05 November 2003

Publication Date:
08 December 2017 (online)

 

 
  • References

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  • 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.