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Thromb Haemost 2000; 83(01): 178-179
DOI: 10.1055/s-0037-1613780
DOI: 10.1055/s-0037-1613780
Letters to the Editor
Genotype Distribution of the 46C/T Polymorphism of Coagulation Factor XII in the Japanese Population: Absence of Its Association with Ischemic Cerebrovascular Disease
Weitere Informationen
Publikationsverlauf
Received
08. September 1999
Accepted
28. September 1999
Publikationsdatum:
27. Dezember 2017 (online)
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References
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- 4 Kanaji T, Okamura T, Osaki K, Kuroiwa M, Shimoda K, Hamasaki N, Niho Y. A common genetic polymorphism (46C to T substitution) in the 5’-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood 1998; 91: 2010-4.
- 5 Kohler HP, Futers TS, Grant PJ. FXII (46C/T) polymorphism and in vivo generation of FXII activity. Thromb Haemost 1999; 81: 745-7.
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