The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change-Reference-Cited by-同舟云学术

The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change

Published:2023-11 Issue: Volume: Page:
ISSN:1538-7836
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:Journal of Thrombosis and Haemostasis

Author:

Christopherson Pamela A.,Tijet Nathalie,Haberichter Sandra L.,Flood Veronica H.,Ross Justyne,Notley Colleen,Rawley Orla,Montgomery Robert R.,James Paula D.,Lillicrap David

Funder

Canadian Institutes of Health Research

National Institutes of Health

NHLBI

Publisher

Elsevier BV

Subject

Hematology

Reference34 articles.

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3. Construction of cDNA coding for human von Willebrand factor using antibody probes for colony-screening and mapping of the chromosomal gene;Verweij;Nucleic Acids Res,1985

4. Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method;Lynch;Cell,1985

5. Updated overview on von Willebrand disease: focus on the interest of genotyping;Itzhar-Baikian;Expert Rev Hematol,2019

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Application of genetic testing for the diagnosis of von Willebrand disease;Journal of Thrombosis and Haemostasis;2024-08

2. Variant p.Tyr1584Cys: a frequent von Willebrand factor variant in search of von Willebrand disease;Research and Practice in Thrombosis and Haemostasis;2024-05