Varaico: Literature-Extracted Genetic Variants

Gene:FGA
Variant:p.V145D
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FGA

NM_021871.4:p.V145D

Associated Papers

Pathogenic Mechanisms in Congenital Afibrinogenemia: A Systematic Review of Genetic Variants.

Li Y et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2025

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.

Mohsenian S et al.

Blood Advances, 2024

Mutations Accounting for Congenital Fibrinogen Disorders: An Update.

Richard M et al.

Seminars in Thrombosis and Hemostasis, 2022

Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.

Mohsenian S et al.

Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."