Varaico: Literature-Extracted Genetic Variants

Gene:F9
Variant:p.L369V
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F9

NM_000133.4:p.L369V

Associated Papers

Evaluation of discrepancy between clot-based and chromogenic factor IX coagulation assays in non-severe hemophilia B patients and identification of the causing mutations.

Mahdavimand M et al.

Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025

Discrepancies between the one-stage clotting assay and the chromogenic assay in haemophilia B.

Kihlberg K et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2017

Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.

Mårtensson A et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2016

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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."