Genetic basis of total kininogen deficiency in Williams' trait.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference32 articles.
1. Chromosomal mapping of human kininogen gene (KNG) to 3q26→qter
2. Structural organization of the human kininogen gene and a model for its evolution.
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2. The First Korean Case of High-Molecular-Weight Kininogen Deficiency, With a Novel Variant, c.488delG, in theKNG1Gene;Annals of Laboratory Medicine;2020-05-01
3. Severe high-molecular-weight kininogen deficiency due to a homozygous c.1456C > T nonsense variant in a large Chinese family;Journal of Thrombosis and Thrombolysis;2020-03-17
4. 2 Molecular and genetic aspects of the kallikrein-kinin system;Kinins;2011-11-16
5. Recombinant Factor XIII Mitigates Hemorrhagic Shock-Induced Organ Dysfunction;Journal of Surgical Research;2011-04
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