Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene-Reference-Cited by-同舟云学术

Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

Published:2000-09 Issue:3 Volume:110 Page:731-734
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Picard Véronique,Bura Alessandra,Emmerich Joseph,Alhenc-Gelas Martine,Biron Christine,Houbouyan-Reveillard Lucie L.,Molho Pascale,Labatide-Alanore Agnès,Sié Pierre,Toulon Pierre,Verdy Elisabeth,Aiach Martine

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2000.02245.x/fullpdf

Reference12 articles.

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2. Inherited anti-thrombin deficiency causing thrombophilia;Egeberg;Thrombosis Diathesis Haemorrhagica,1965

3. Three novel mutations of anti-thrombin inducing high-molecular-mass compounds;Emmerich;Arteriosclerosis and Thrombosis,1994

4. Congenital anti-thrombin III deficiency. Incidence and clinical features;Hirsh;American Journal of Medicine,1989

5. Implication of the three dimensional structure of α1-antitrypsin for structure and function of serpins;Huber;Biochemistry,1989

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