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- W2415175216 abstract "Summary Three cases of true congenital hypoprothrombinaemia are presented. Studies were made to prove the deficiency of prothrombin in the patient’s plasma and to rule out deficiency of other clotting factors or the presence of abnormal anti-thrombin substances. All the patients were of group B. The results obtained confirm that the patients have a real prothrombin deficiency as the cause of a severe haemorrhagic disease." @default.
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- W2415175216 date "1964-01-01" @default.
- W2415175216 modified "2023-09-26" @default.
- W2415175216 title "A Study of Three Cases of Familial Congenital Hypoprothrombinaemia (Factor II Deficiency)" @default.
- W2415175216 doi "https://doi.org/10.1055/s-0038-1654845" @default.
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