Associated Papers
Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence.
Adenaeuer A et al.
Journal of Thrombosis and Haemostasis : Jth, 2023
The First Korean Case of High-Molecular-Weight Kininogen Deficiency, With a Novel Variant, c.488delG, in the KNG1 Gene.
Jeong D et al.
Annals of Laboratory Medicine, 2020
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