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Novel ADAMTS-13 mutations in an adult with delayed onset thrombotic thrombocytopenic purpura

✍ Scribed by Z. TAO; K. ANTHONY; Y. PENG; H. CHOI; L. NOLASCO; L. RICE; J. L. MOAKE; J.-F. DONG


Book ID
109151690
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
564 KB
Volume
4
Category
Article
ISSN
1538-7933

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ADAMTS13 mutations and polymorphisms in
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Congenital thrombotic thrombocytopenic purpura (TTP) (also known as Upshaw-Schulman syndrome, USS) is a rare, life-threatening disease characterized by thrombocytopenia and microangiopathic hemolytic anemia, associated with the deficiency of the von Willebrand factor-cleaving protease (ADAMTS13) due