F8 A3-C1-C2 variants defective in phospholipid binding. [extracellular region]

Stable Identifier
R-HSA-9670218
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
25354705 Molecular simulation studies of human coagulation factor VIII C domain-mediated membrane binding

Du, J, Wichapong, K, Hackeng, KM, Nicolaes, GA

Thromb. Haemost. 2015
15471879 Surface-exposed hemophilic mutations across the factor VIII C2 domain have variable effects on stability and binding activities

Spiegel, PC, Murphy, P, Stoddard, BL

J. Biol. Chem. 2004
Participants
Participant Of
Disease
Name Identifier Synonyms
factor VIII deficiency 12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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