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

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Thromb Haemost 2000; 84(06): 1126
DOI: 10.1055/s-0037-1614187

Letters to the Editor

Schattauer GmbH

Ichiro Fuse

¹First Department of Internal Medicine, Niigata University School of Medicine, Japan

,

Tetsuo Ozawa

²Department of Clinical and Laboratory Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan

,

Wataru Higuchi

¹First Department of Internal Medicine, Niigata University School of Medicine, Japan

,

Yoshifusa Aizawa

¹First Department of Internal Medicine, Niigata University School of Medicine, Japan

Weitere Informationen

Publikationsverlauf

Received 03. Mai 2000

Accepted after resubmission 24. Juli 2000

Publikationsdatum:
13. Dezember 2017 (online)

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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