Varaico: Literature-Extracted Genetic Variants

Gene:VWF
Variant:p.R1308S
Back to variants list

VWF

NM_000552.5:p.R1308S

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

Diagnosing Inherited Platelet Disorders: Modalities and Consequences.

Zaninetti C et al.

Hamostaseologie, 2021

A family having type 2B von Willebrand disease with a novel VWF p.R1308S mutation: Detection of characteristic platelet aggregates on peripheral blood smears as the key aspect of diagnosis.

Hatta K et al.

Thrombosis Research, 2015

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."