Hemofília

Haemophilia B Mutation Database Version 13 2004 A database of point mutations and short additions and deletions in the factor IX gene

FVII Facts

Molecular weight

primary translation product - 466 amino acids or 444 amino acids depending on usage of exon 1b
mature protein - 406 amino acids
predicted molecular weight - 45078 (light chain: 17025; heavy chain: 28053)
SDS PAGE - approximately 50,000 kDa

HAMSTeRS
The Haemophilia A Mutation, Structure, Test and Resource Site

Up-to-date databases of point mutations, insertions, deletions, and polymorphisms found in the gene for human von Willebrand Factor.

RARE BLEEDING DISORDER DATABASE
Rare bleeding disorders (RBDs) are very rare diseases, relatively neglected until recently by health care providers, advocacy organizations and pharmaceutical companies. Haemophilia A and B are the most frequent inherited bleeding disorders. Together with von Willebrand disease, a defect of primary hemostasis associated with a secondary defect in coagulation factor VIII (FVIII), these X-linked disorders include 95% to 97% of all the inherited deficiencies of coagulation factors

FXIII Registry Database
Introduction to FXIII Deficiency

IntReAVWS
On behalf of the Scientific Subcommittee on vWF
The acquired von Willebrand syndrome (AVWS) is a rare bleeding disorder with laboratory findings similar to those for congenital von Willebrand disease.

databáze mutácií f VIII a f VII

Rare Bleeding Disorders Database
Databáza vzácnych krvácavých ochorení