Clinical utility of panel-based genetic sequencing for von Willebrand disease

Clinical utility of panel-based genetic sequencing for von Willebrand disease

Background: von Willebrand disease (VWD) is the most prevalent inherited bleeding disorder with a wide spectrum of causative variants. Next-generation sequencing analyzes the entire VWF gene and provides concomitant assessment of other genes, allowing differentiation between genocopies. Objectives:...

Full description

Saved in:
Bibliographic Details
Main Authors: Radha Ramanan, Christine Van Laer, Sarissa Baert, Cyrielle Kint, Chris Van Geet, Quentin Van Thillo, Peter Verhamme, Thomas Vanassche, James D. McFadyen, Andrew C. Perkins, Huyen A. Tran, Veerle Labarque, Kathleen Freson
Format: Article
Language:English
Published: Elsevier 2025-02-01
Series:Research and Practice in Thrombosis and Haemostasis
Subjects:
genotype
high-throughput nucleotide sequencing
phenotype
von Willebrand diseases
Online Access:http://www.sciencedirect.com/science/article/pii/S2475037925000548
Tags: Add Tag
No Tags, Be the first to tag this record!
Be the first to leave a comment!
You must be logged in first

Similar Items