Diagnostic du déficit en protéine S
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry
Reference44 articles.
1. Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families;Andersen;Thromb Haemost,2001
2. Maturation of the hemostatic system during childhood;Andrew;Blood,1992
3. Molecular bases of type II protein S deficiency: the I203–D204 deletion in the EGF4 domain alters Gla domain function;Baroni;J Thromb Haemost,2006
4. Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French network on molecular abnormalities responsible for protein C and protein S deficiencies;Borgel;J Lab Clin Med,1996
5. First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484–>Pro, in the protein S active gene (PROS1);Borgel;Thromb Haemost,1996
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spontaneous miscarriages and congenital protein S deficiency: a case report;Annales de biologie clinique;2013-03
2. Thrombose de la veine cave supérieure révélatrice d’un déficit de la protéine S. À propos d’un cas;Revue de Pneumologie Clinique;2012-12
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