Varaico: Literature-Extracted Genetic Variants

Gene:FGG
Variant:p.K121*
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FGG

NM_021870.3:p.K121*

Associated Papers

Mutations Accounting for Congenital Fibrinogen Disorders: An Update.

Richard M et al.

Seminars in Thrombosis and Hemostasis, 2022

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.

Naz A et al.

Thrombosis Journal, 2019

Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders.

Tiscia GL et al.

International Journal of Molecular Sciences, 2018

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.

Naz A et al.

Thrombosis Journal, 2017

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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."