Hereditary factor V deficiency from heterozygous mutations with a novel variant p.Pro798Leufs∗13 in the F5 gene-Reference-Cited by-同舟云学术

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Hereditary factor V deficiency from heterozygous mutations with a novel variant p.Pro798Leufs∗13 in the F5 gene

Published:2021-06-07 Issue:7 Volume:32 Page:513-518
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Deng Yuping,Zhu Jiajin,Gong Yuxiang,Yi Xiaoqing,Zhou Liyan,Xie Yaosheng,Wang Mingshan,Wu Wenhe

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference16 articles.

1. Structure of the gene for human coagulation factor V;Cripe;Biochemistry,1992

2. Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency;Cutler;Haemophilia,2010

3. In vitro’ correction of the severe factor V deficiency-related coagulopathy by a novel plasma-derived factor V concentrate;Bulato;Haemophilia,2018

4. A comprehensive overview of coagulation factor V and congenital factor V deficiency;Tabibian;Semin Thromb Hemost,2019

5. Profiling the mutational landscape of coagulation factor V deficiency;Paraboschi;Haematologica,2020

Cited by 1 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 Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations;Hämostaseologie;2023-06-15

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