Blood coagulation factor VIII: An overview.
J Biosci
; 2003 Dec; 28(6): 783-9
Article
de En
| IMSEAR
| ID: sea-110831
Factor VIII (FVIII) functions as a co-factor in the blood coagulation cascade for the proteolytic activation of factor X by factor IXa. Deficiency of FVIII causes hemophilia A, the most commonly inherited bleeding disorder. This review highlights current knowledge on selected aspects of FVIII in which both the scientist and the clinician should be interested.
Texte intégral:
1
Indice:
IMSEAR
Sujet Principal:
Humains
/
Facteur VIII
/
Hémophilie A
/
Mutation
langue:
En
Texte intégral:
J Biosci
Année:
2003
Type:
Article