Hemophilia is caused by mutations in either the factor VIII (FVIII) or factor IX (FIX) genes, classified as hemophilia A and hemophilia B, respectively. Both genes are located on the X chromosome, causing the classic X-linked inheritance of these conditions. The comprehensive incidence of ...
Pathophysiology of the disturbed angiogenesis in hemophiliaHemophiliaangiogenesisantiangiogenic drugshemarthrosishemophilic arthropathyIntroduction: It has been reported an increase ofdoi:10.1080/17474086.2016.1234933CarlosLaRodriguez-MerchanLaE.LaExpert review of hematology...