Isolated high-molecular-weight kininogen deficiency: a novel frameshift mutation in exon 10-Reference-Cited by-同舟云学术

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Isolated high-molecular-weight kininogen deficiency: a novel frameshift mutation in exon 10

Published:2007-06-01 Issue:11 Volume:109 Page:5062-5063
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Shigekiyo Toshio,Miyagi Junko,Shirakami Atsuhisa,Shibata Hironobu,Tsukai Kazuo,Aihara Ken-ichi

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/109/11/5062/1479933/zh801107005062.pdf

Reference6 articles.

1. Characterization of molecular defects of Fitzgerald trait and another novel high-molecular-weight kininogen-deficient patient: insights into structural requirements for kininogen expression.;Krijanovski;Blood,2003

2. Molecular genetic survey of five Japanese families with high-molecular-weight kininogen deficiency.;Hayashi;Blood,1990

3. A case of Fitzgerald factor (High molecular weight kininogen) deficiency: the third family in Japan [Japanese].;Tsukai;Tokushima J Med,1984

4. Differential assay for high molecular weight and low molecular weight kininogens.;Uchida;Thromb Res,1979

5. Structural organization of the kininogen gene and a model for its evolution.;Kitamura;J Biol Chem,1985

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. Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency–causing KNG1 variants, and estimated prevalence;Journal of Thrombosis and Haemostasis;2023-02

2. A Novel Frameshift Mutation in Exon 4 Causing a Deficiency of High-molecular-weight Kininogen in a Patient with Splenic Infarction;Internal Medicine;2014

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