Varaico: Literature-Extracted Genetic Variants

Gene:FGA
Variant:p.W60_N61Splc
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FGA

NM_021871.4:p.W60_N61Splc

Associated Papers

Clinical phenotype and laboratory characteristics of 93 patients with congenital fibrinogen disorders from unrelated 36 families.

Tian D et al.

Research and Practice in Thrombosis and Haemostasis, 2024

Mutations Accounting for Congenital Fibrinogen Disorders: An Update.

Richard M et al.

Seminars in Thrombosis and Hemostasis, 2022

Rare coagulation deficiencies.

Peyvandi F et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2002

Autosomal recessive deficiencies of coagulation factors.

Peyvandi F et al.

Reviews in Clinical and Experimental Hematology, 2001

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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."