Identification of simultaneous mutation of fibrinogen α chain and protein C genes in a Japanese kindred-Reference-Cited by-同舟云学术

Identification of simultaneous mutation of fibrinogen α chain and protein C genes in a Japanese kindred

Published:2002-12-20 Issue:1 Volume:120 Page:101-108
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Watanabe Kumiko,Shibuya Atsushi,Ishii Eiichi,Kurihara Masako,Inoue Sumiko,Ono Miyuki,Wada Yui,Wakiyama Machiko,Zaitsu Masafumi,Iida Hiroko,Muraoka Kenji,Kinoshita Sachiko,Hamasaki Naotaka

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2003.03985.x/fullpdf

Reference31 articles.

1. Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation;Asselta;Blood,2000

2. Congenital abnormalities of fibrinogen;Beck;Clinical Haematology,1979

3. Identification of mutations in 15 Hungarian families with hereditary protein C deficiency;David;British Journal of Haematology,2000

4. Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion;Duga;Blood,2000

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4. siRNA down-regulation of FGA mRNA in HepG2 cells demonstrated that heterozygous abnormality of the Aα-chain gene does not affect the plasma fibrinogen level;Thrombosis Research;2013-04

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