Varaico: Literature-Extracted Genetic Variants

Gene:FGA
Variant:p.G32*
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FGA

NM_021871.4:p.G32*

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

Establishment and genetic characterization of zebrafish RW line.

Sadamitsu K et al.

Scientific Reports, 2025

40281206 (PubMed )
Supplement: 41598_2025_98674_MOESM2_ESM.xlsx › Table_S3__TL_

Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia.

Simurda T et al.

International Journal of Hematology, 2020

Congenital fibrinogen disorders: an update.

de Moerloose P et al.

Seminars in Thrombosis and Hemostasis, 2013

Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.

Neerman-Arbez M et al.

Human Mutation, 2007

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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."