Genetic defects in von Willebrand disease type 3 in Indian and Greek patients
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference33 articles.
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3. Human von Willebrand factor gene and pseudogene structural analysis and differentiation by polymerase chain reaction;Mancuso;Biochemistry,1991
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1. Genotyping R1336X and Eliminating the Pseudogene Amplification in Type 3 von Willebrand Disease Patients;Indian Journal of Hematology and Blood Transfusion;2024-06-24
2. von Willebrand factor propeptide variants lead to impaired storage and ER retention in patient‐derived endothelial colony‐forming cells;Journal of Thrombosis and Haemostasis;2022-07
3. A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies;International Journal of Molecular Sciences;2022-03-13
4. Variants p.Pro2063Ser and p.Arg324* co‐segregate in type 3 von Willebrand disease patients from Southern Brazil;Haemophilia;2021-02-06
5. The Current Understanding of Molecular Pathogenesis of Quantitative von Willebrand Disease, Types 1 and 3;Hämostaseologie;2020-01-22
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