Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency-Reference-Cited by-同舟云学术

Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency

Published:2019-12 Issue:8 Volume:30 Page:413-418
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Zhou Xingxing,Zhang Haiyue,Wang Mingshan,Luo Shasha,Liu Siqi,Jin Yanhui,Li Xiaolong,Yang Lihong

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference10 articles.

1. Bleeding phenotype and correlation with factor XI (FXI) activity in congenital FXI deficiency: results of a retrospective study from a single centre;Santoro;Haemophilia,2015

2. The gene analysis of a Chinese pedigree with congenital blood coagulation factor XI deficiency;Dai;J Wenzhou Med Univ,2015

3. A novel mutation (Tyr503Cys) in a severe factor XI deficiency;Su;Blood Coagul Fibrinolysis,2018

4. Identification of two novel factor XI nonsense mutation Trp228stop and Trp383stop in a Chinese pedigree of congenital factor XI deficiency;Wu;Zhonghua Xue Ye Xue Za Zhi,2003

5. Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians;Zadra;Haematologica,2008

Cited by 2 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. Gene Variants in Two Families with Inherited Coagulation Factor XI Deficiency and Identification of Mutations;Acta Haematologica;2022-12-21

2. Detection and Gene Mutation Analysis of Three Variations in Two Unrelated Chinese Hereditary Coagulation Factor XI Deficiency Families;Acta Haematologica;2022