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- W2044202959 abstract "The authors describe a 12-year-old girl with late-onset clinical symptoms due to severe protein C deficiency. Protein C gene analysis showed double heterozygosity for two distinct mutations, associated with type I protein C deficiency. Her parents and only brother were also evaluated. Coumarin-induced skin necrosis was a recurrent feature during oral anticoagulation therapy, forcing her physicians to treat her with nadroparin (Fraxiparin) for only a few months." @default.
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- W2044202959 date "2004-01-01" @default.
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- W2044202959 title "Late Onset of Clinical Symptoms and Recurrent Ecchymotic Skin Lesions in a 12-Year-Old Girl With a Severe Double Heterozygous Protein C Deficiency" @default.
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- W2044202959 doi "https://doi.org/10.1097/00043426-200401000-00002" @default.
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