Ontology highlight
ABSTRACT:
SUBMITTER: Valjevac A
PROVIDER: S-EPMC4333927 | biostudies-literature | 2013 Feb
REPOSITORIES: biostudies-literature
Valjevac Amina A Mehić Bakir B Kiseljaković Emina E Ibrulj Slavka S Garstka Agnieszka A Adler Grażyna G
Bosnian journal of basic medical sciences 20130201 1
Factor V is the liver-synthesized multidomain glycoprotein encoded by a gene localised on chromosome 1q23. The point mutation 1691G>A in this gene results in formation of an altered protein of V Factor resistant to activated protein C (APC) cleavage. This mutation alone is the most frequent cause of inborn thrombophilia and the most widely acknowledged genetic risk factor for venous thrombosis in a Caucasian population. This study was designed to provide the first estimate of the frequency of th ...[more]