Download PDF
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
› Author Affiliations
Further Information

Publication History

Received 03 May 2000

Accepted after resubmission 24 July 2000

Publication Date:
13 December 2017 (online)

    Permissions and Reprints

 

 

  • 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.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 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.
    Article in Thieme ConnectPubMedGoogle Scholar