Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIII A subunit-Reference-Cited by-同舟云学术

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Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIII A subunit

Published:1997-08 Issue:2 Volume:98 Page:346-352
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Aslam S.¹,Yee V. C.²,Narayanan S.³,Duraisamy G.⁴,Standen G. R.¹

Affiliation:

1. Molecular Haematology Unit, Department of Haematology, Bristol Royal Infirmary, Bristol, U.K.,

2. Departments of Biochemistry and Biological Structure, University of Washington, Seattle, Washington, U.S.A.,

3. Department of Paediatrics, Princess Margaret Hospital, Swindon, U.K.,

4. National Blood Services Centre, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2141.1997.2263043.x

Cited by 19 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. Genetic landscape in coagulation factor XIII associated defects – Advances in coagulation and beyond;Blood Reviews;2023-05

2. Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function;Annals of Hematology;2014-06-03

3. Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations;Haemophilia;2013-12-16

4. Factor XIII Deficiency: An Update;Seminars in Thrombosis and Hemostasis;2013-08-08

5. An update of the mutation profile of Factor 13 A and B genes;Blood Reviews;2011-09

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