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- W2911953808 abstract "Prothrombin (factor II) deficiency is a rare congenital inherited bleeding disorders affecting 1/2000 000 subjects. The disorder is characterized by a wide range of phenotypes from asymptomatic cases to patients suffering from life-threatening bleeds at a young age. A complete deficiency of the protein is presumably incompatible with life. Despite progress over the years, several issues remain to be clarified in the diagnosis and management of patients. Due to the low prevalence of the disease, activities such as international collaborations and databases should therefore be encouraged and supported." @default.
- W2911953808 created "2019-02-21" @default.
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- W2911953808 date "2014-04-24" @default.
- W2911953808 modified "2023-09-29" @default.
- W2911953808 title "Factor II" @default.
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- W2911953808 doi "https://doi.org/10.1002/9781118398258.ch54" @default.
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