Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes-Reference-Cited by-同舟云学术

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Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes

Published:2008-04 Issue:3 Volume:19 Page:247-253
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Simsek Ismail,de Mazancourt Philippe,Horellou Marie-Hèléne,Erdem Hakan,Pay Salih,Dinc Ayhan,Samama Meyer Michel

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference38 articles.

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

2. Congenital dysfibrinogenemia;Martinez;Curr Opin Hematol,1997

3. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia;Lak;Br J Haematol,1999

4. Rare coagulation disorders;Peyvandi;Thromb haemost,1999

5. Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion;Kant;Proc Natl Acad Sci U S A,1985

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3. Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria;Haemophilia;2022-04-30

4. Extension of the Human Fibrinogen Database with Detailed Clinical Information—The αC-Connector Segment;International Journal of Molecular Sciences;2021-12-23

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