Research of Factor X Deficiency has been linked to Hemorrhage, Inherited Factor Ii Deficiency, Blood Coagulation Disorders, Amyloidosis, Factor Vii Deficiency. The study of Factor X Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Factor X Deficiency include Coagulation, Blood Coagulation, Hemostasis, Platelet Aggregation, Fibrinolysis. These pathways complement our catalog of research reagents for the study of Factor X Deficiency including antibodies and ELISA kits against FACTOR VIII, FVII, STUART FACTOR, FACTOR XII, THROMBIN.
Factor X Deficiency Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Factor X Deficiency below!
For more information on how to use Laverne, please read the How to Guide.
We have 614 products for the study of Factor X Deficiency that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Factor X Deficiency is also known as factor x deficiency, stuart-prower factor deficiency, factor x deficiency (disorder), stuart factor deficiency, congenital, factor x deficiency, congenital, disease, stuart-prower, f10 deficiency.