The molecular genetic analysis of familial venous thrombosis

Cooper, David Neil ORCID: https://orcid.org/0000-0002-8943-8484 1991. The molecular genetic analysis of familial venous thrombosis. Blood Reviews 5 (1) , pp. 55-70. 10.1016/0268-960X(91)90009-2

Full text not available from this repository.

Abstract

Inherited defects of antithrombin III, protein C, protein S, heparin cofactor II, plasminogen and the fibrinogens are thought to be responsible for between 10 and 15% of all patients presenting with recurrent venous thrombosis. The structure, function and expression of these genes and the nature of the gene lesions underlying the deficiency states are reviewed in detail.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Schools > Medicine
Subjects:	R Medicine > R Medicine (General)
Publisher:	Elsevier
ISSN:	0268-960X
Last Modified:	31 Oct 2022 10:12
URI:	https://orca.cardiff.ac.uk/id/eprint/84015

Actions (repository staff only)

Edit Item