R924Q substitution encoded within exon 21 of the von Willebrand Factor gene related to mild bleeding phenotype-Reference-Cited by-同舟云学术

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R924Q substitution encoded within exon 21 of the von Willebrand Factor gene related to mild bleeding phenotype

Published:2006 Issue:08 Volume:96 Page:228-230
ISSN:0340-6245
Container-title:Thrombosis and Haemostasis
language:en
Short-container-title:Thromb Haemost

Author:

Woods Adriana,Kempfer Ana,Farías Cristina,Grosso Silvia,Lazzari María,Casais Patricia,Carballo Gonzalo

Funder

René Barón Foundation

National Research Council (CONICET)

Science and Technology Secretary (SECYT)

Publisher

Georg Thieme Verlag KG

Subject

Hematology

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH06-03-0144.pdf

Cited by 10 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. Clinical relevance of genetic variants in the von Willebrand factor according to in‐silico methods;American Journal of Medical Genetics Part A;2023-10-23

2. Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS;Blood Advances;2021-08-05

3. The D′ domain of von Willebrand factor requires the presence of the D3 domain for optimal factor VIII binding;Biochemical Journal;2018-09-11

4. Clinical profile of the association of P.R1205h and P.R924q in a patient with von Willebrand's disease;Haemophilia;2013-03-13

5. Diagnosis and Management ofvon Willebrand Disease in a Single Institution of Argentina;Seminars in Thrombosis and Hemostasis;2011-07

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