Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.

Details

Serval ID
serval:BIB_45C37BEC9E59
Type
Article: article from journal or magazin.
Collection
Publications
Title
Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.
Journal
Thrombosis and Haemostasis
Author(s)
Alatri A., Franchi F., Moia M.
ISSN
0340-6245 (Print)
ISSN-L
0340-6245
Publication state
Published
Issued date
1998
Volume
80
Number
6
Pages
1028-1029
Language
english
Notes
Publication types: Case Reports ; Letter
Keywords
3' Untranslated Regions, Adult, Aged, Brain Ischemia/blood, Brain Ischemia/etiology, Female, Genetic Predisposition to Disease, Homocysteine/blood, Homozygote, Humans, Male, Methionine/diagnostic use, Middle Aged, Prothrombin/genetics, Risk Factors, Thrombophilia/epidemiology, Thrombophilia/genetics, Thrombophlebitis/blood, Thrombophlebitis/etiology
Pubmed
Web of science
Create date
14/02/2013 12:59
Last modification date
03/06/2020 5:26
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