Varaico: Literature-Extracted Genetic Variants

Gene:VWF
Variant:p.L1365P
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VWF

NM_000552.5:p.L1365P

Associated Papers

Landscape and Spectrum of VWF Variants in Type 2 Von Willebrand Disease: Insights from a German Patient Cohort.

Yadegari H et al.

Thrombosis and Haemostasis, 2026

von Willebrand Factor (VWF) Inhibitors in Two Brothers with von Willebrand Disease: A Case Report.

Djambas Khayat C et al.

Th Open : Companion Journal to Thrombosis and Haemostasis, 2025

Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.

Preisler B et al.

Journal of Clinical Medicine, 2021

Comprehensive re-evaluation of historical von Willebrand disease diagnosis in association with whole blood platelet aggregation and function.

Nummi V et al.

International Journal of Laboratory Hematology, 2018

Collagen binding provides a sensitive screen for variant von Willebrand disease.

Flood VH et al.

Clinical Chemistry, 2013

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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."