Variants leading to dysfibrinogenaemia in the fibrinogen α‐chain at residue Arg19 are not solely associated with bleeding, but also with thrombotic events

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Variants leading to dysfibrinogenaemia in the fibrinogen α‐chain at residue Arg19 are not solely associated with bleeding, but also with thrombotic events—RESPONSE

Published:2024-04-12 Issue:6 Volume:204 Page:2504-2504
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Ramanan Radha¹²³^ORCID,McFadyen James D.¹²⁴,Perkins Andrew C.¹²³^ORCID,Tran Huyen A.¹²^ORCID

Affiliation:

1. Department of Haematology Alfred Hospital Melbourne Victoria Australia

2. Australian Centre for Blood Diseases Monash University Melbourne Victoria Australia

3. Department of Pathology Alfred Hospital Melbourne Victoria Australia

4. Atherothrombosis and Vascular Biology Program Baker Heart and Diabetes Institute Melbourne Victoria Australia

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.19431

Reference5 articles.

1. Congenital fibrinogen disorders: Strengthening genotype–phenotype correlations through novel genetic diagnostic tools

2. Dysfibrinogenemia—potential impact of genotype on thrombosis or bleeding;Bor MVF;Semin Thromb Hemost,2021

3. A Database for Human Fibrinogen Variants

4. Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing

5. Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

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