Varaico: Literature-Extracted Genetic Variants

Gene:VWF
Variant:p.S2559insFs
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VWF

NM_000552.5:p.S2559insFs

Associated Papers

Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.

Baronciani L et al.

Blood Advances, 2021

Molecular Characterization of Iranian Patients with Inherited Coagulation Factor VII Deficiency.

S S et al.

Balkan Journal of Medical Genetics : Bjmg, 2017

Nonsense-mediated mRNA decay among coagulation factor genes.

Shahbazi S

Iranian Journal of Basic Medical Sciences, 2016

Nonsense mediated decay of VWF mRNA subsequent to c.7674-7675insC mutation in type3 VWD patients.

Shahbazi S et al.

Blood Cells, Molecules & Diseases, 2012

Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients.

Baronciani L et al.

Blood Cells, Molecules & Diseases, 0

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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."