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

Authors

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

Received 03 May 2000

Accepted after resubmission 24 July 2000

Publication Date:
13 December 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.

Reference Link Ris
Thieme Connect PubMed Search in Google Scholar