Varaico: Literature-Extracted Genetic Variants

Gene:F11
Variant:p.I426T
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F11

NM_000128.4:p.I426T

Associated Papers

Anticoagulant therapy in patients with congenital FXI deficiency.

Bravo-Pérez C et al.

Blood Advances, 2021

Assessment of two contact activation reagents for the diagnosis of congenital factor XI deficiency.

Salloum-Asfar S et al.

Thrombosis Research, 2018

High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.

Esteban J et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 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."