Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha‐2‐antiplasmin deficiency-Reference-Cited by-同舟云学术

Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha‐2‐antiplasmin deficiency

Published:2019-07-08 Issue:6 Volume:186 Page:
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Egan Grace¹^ORCID,Pluthero Fred G.²^ORCID,Bouskill Vanessa³,Hilliard Pamela⁴,Drury Luke J.⁵,Carcao Manuel D.¹⁴^ORCID,Kahr Walter H. A.¹²⁶^ORCID

Affiliation:

1. Division of Haematology/Oncology, Department of Paediatrics The Hospital for Sick Children and University of Toronto Toronto ON Canada

2. Cell Biology Program, Research Institute The Hospital for Sick Children Toronto ON Canada

3. Department of Nursing The Hospital for Sick Children Toronto ON Canada

4. Child Health Evaluative Sciences Program, Research Institute The Hospital for Sick Children Toronto ON Canada

5. Prevention Genetics Marshfield WI USA

6. Department of Biochemistry University of Toronto Toronto ON Canada

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16077

Reference10 articles.

1. Natural heterogeneity of α2-antiplasmin: functional and clinical consequences

2. Congenital Deficiency of α2-Plasmin Inhibitor Associated with Severe Hemorrhagic Tendency *

3. α2-Antiplasmin and its deficiency: fibrinolysis out of balance

4. Congenital α2-plasmin inhibitor deficiencies: a review

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