Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy-Reference-Cited by-同舟云学术

Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy

Published:1997-07 Issue:1 Volume:98 Page:240-244
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Oldenburg Johannes¹²,Quenzel Ernst‐Markus²,Harbrecht Uschi²,Fregin Andreas¹,Kress Wolfram¹,Müller Clemens Rainer¹,Hertfelder Hans‐Jörg²,Schwaab Rainer²,Brackmann Hans‐Hermann²,Hanfland Peter²

Affiliation:

1. Department of Human Genetics, University of Würzburg, Biocentre, Am Hubland, Würzburg,

2. Department of Experimental Haematology and Transfusion Medicine, University of Bonn, Bonn, Germany

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2141.1997.2213036.x

Cited by 76 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. Multiplex, multimodal mapping of variant effects in secreted proteins;2024-04-01

2. Hemophilia B: Diagnosis and Management;Congenital Bleeding Disorders;2023

3. Factor IX p.A37V mutation causes severe bleeding in a patient with phenprocoumon therapy;European Journal of Medical Research;2021-06-29

4. Clinical Problem Solving and Using New Paths in the Laboratory: Learning from Case Studies;Hämostaseologie;2020-08-20

5. Severe bleeding due to hypersensitivity to vitamin K antagonist caused by the c.109G>A (p.Ala37Thr) mutation in the F9 gene in a patient with mechanical heart valve prosthesis;Thrombosis Research;2019-02