A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene-Reference-Cited by-同舟云学术

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A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene

Published:2021-05 Issue:4 Volume:5 Page:
ISSN:2475-0379
Container-title:Research and Practice in Thrombosis and Haemostasis
language:en
Short-container-title:Res Pract Thromb Haemost

Author:

Mansory Eman M.¹²,Bhai Pratibha³,Stuart Alan³,Laudenbach Lori⁴,Sadikovic Bekim³,Lazo‐Langner Alejandro¹⁵^ORCID

Affiliation:

1. Division of Hematology Department of Medicine Western University London ON Canada

2. Department of Hematology King Abdulaziz University Jeddah Saudi Arabia

3. Molecular Diagnostics Division Department of Pathology and Laboratory Medicine Western University London ON Canada

4. Bleeding Disorders Program London Health Sciences Program London ON Canada

5. Department of Epidemiology and Biostatistics Western University London ON Canada

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rth2.12510

Reference19 articles.

1. Congenital Prothrombin Deficiency: An Update

2. Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed

3. Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

4. A novel congenital dysprothrombinemia leading to defective prothrombin maturation

5. A severe neonatal presentation of factor II deficiency

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