Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III-Reference-Cited by-同舟云学术

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Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III

Published:1992 Issue:1 Volume:1 Page:61-62
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Zhang Z.P.,Falk G.,Blombäck M.,Egberg N.,Anvret M.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/1/1/61/1970898/1-1-61.pdf

Cited by 29 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. Variants p.Pro2063Ser and p.Arg324* co‐segregate in type 3 von Willebrand disease patients from Southern Brazil;Haemophilia;2021-02-06

2. Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia;British Journal of Haematology;2017-07-27

3. Clinical, Laboratory, and Molecular Markers of Type 3 von Willebrand Disease;Von Willebrand Disease;2011-03-21

4. Two new candidate mutations in type IIA von Willebrand's disease (ARG834→GLY, GLY846→ARG) and one polymorphism (TYR821→CYS) in the A2 region of the von Willebrand factor;European Journal of Haematology;2009-04-24

5. Genetic polymorphism in a region of the vWF pseudogene corresponding to exon 28 of the vWF gene;European Journal of Haematology;2009-04-24

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