Author:
Pintao Maria C.,Garcia A. A.,Borgel D.,Alhenc-Gelas M.,Spek C. A.,de Visser M. C. H.,Gandrille S.,Reitsma Pieter H.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference39 articles.
1. Bertina RM (1990) Nomenclature proposal for protein S deficiency. XXXVI Annual meeting of Scientific and Standardization Committee of the International Society for Thrombosis and Haemostasis, June; Barcelona, Spain
2. Borgel D, Duchemin J, Alhenc-Gelas M, Matheron C, Aiach M, Gandrille S (1996) 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. J Lab Clin Med 128:218–227
3. Choung HS, Kim HJ, Gwak GY, Kim SH, Kim DK (2008) Inherited protein S deficiency as a result of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification. J Thromb Haemost 6:1430–1432
4. Comp PC, Doray D, Patton D, Esmon CT (1986) An abnormal plasma distribution of protein S occurs in functional protein S deficiency. Blood 67:504–508
5. Dahlbäck B (2000) Blood coagulation. Lancet 355:1627–1632
Cited by
36 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