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Thromb Haemost 2000; 84(06): 1126
DOI: 10.1055/s-0037-1614187
Letters to the Editor
Schattauer GmbH

Antithrombin Niigata: A Novel Missense Mutation (Thrl94-lle) of the Antithrombin Gene Results in Type I Deficiency

Ichiro Fuse
1   First Department of Internal Medicine, Niigata University School of Medicine, Japan
,
Tetsuo Ozawa
2   Department of Clinical and Laboratory Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan
,
Wataru Higuchi
1   First Department of Internal Medicine, Niigata University School of Medicine, Japan
,
Yoshifusa Aizawa
1   First Department of Internal Medicine, Niigata University School of Medicine, Japan
› Institutsangaben
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Publikationsverlauf

Received 03. Mai 2000

Accepted after resubmission 24. Juli 2000

Publikationsdatum:
13. Dezember 2017 (online)

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  • References

  • 1 Ozawa T, Sakuragawa N. Genetic analysis of mutations in seven Japanese families with type I antithrombin deficiency. Semin Thromb Hemost 1998; 24: 233-6.
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  • 2 Lane DA, Bayston T, Olds RJ, Pitches AC, Cooper DN, Millar DS, Jochmans K, Perry DJ, Okajima K, Thein SL. Emmerich J: Antithrombin mutation database: 2nd (1997) update. Thromb Haemost 1997; 77: 197-211.
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