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Child‐onset thrombotic thrombocytopenic purpura caused by p.R498C and p.G259PfsX133 mutations in ADAMTS13

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Patients suffering from congenital thrombotic thrombocytopenic purpura (cTTP) have a deficiency in ADAMTS13 due to mutations in their ADAMTS13 gene.
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Keywords: ADAMTS13; mutation; thrombotic thrombocytopenic purpura

Document Type: Research Article

Publication date: August 1, 2018

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