Two novel mutations in ADAMTS13 in a Chinese boy with congenital thrombocytopenic purpura: a case report
Abstract Background Mutations in the ADAMTS13 gene family have been reported to cause congenital thrombotic thrombocytopenic purpura (cTTP), a rare disease characterized by thrombocytopenia and hemolytic anemia. Nearly 150 causative mutations in ADAMTS13 have been identified; however, only a few of...
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| Main Authors: | , |
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| Format: | Book |
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BMC,
2020-03-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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