NovelADAMTS13mutations in an obstetric patient with Upshaw-Schulman syndrome
Author:
Affiliation:
1. Department of Pathology; University of Alabama at Birmingham; Birmingham; Alabama
2. Department of Hematology and Central Hematology Laboratory, Inselspital; Berne University Hospital and University of Berne; Berne; Switzerland
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jca.21251/fullpdf
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2. The incidence of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS-13 deficiency;Terrell;J Thromb Haemost,2005
3. Clinical practice. Thrombotic thrombocytopenic purpura;George;N Engl J Med,2006
4. Correction of ADAMTS13 deficiency by in utero gene transfer of lentiviral vector encoding ADAMTS13 genes;Niiya;Mol Ther,2009
5. Thrombotic microangiopathies;Moake;N Engl J Med,2002
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2. Diagnosis of Hereditary TTP Caused by Homozygosity for a Rare Complex ADAMTS13 Allele After Salmonella Infection in a 43-Year-Old Asylum Seeker;Frontiers in Medicine;2021-02-26
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