Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family-Reference-Cited by-同舟云学术

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Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family

Published:2018-01-07 Issue:8 Volume:23 Page:501-509
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Sun Liwei¹,Yan Qijiang²,Wang Yonghua¹,Luo Hualei¹,Du Peng¹,Hassan Reem¹,Liu Li³,Jiang Weiying¹

Affiliation:

1. Department of Medical Genetics, ZhongShan School of Medicine, Sun Yat-sen University, Guangzhou, People’s Republic of China

2. Guangzhou Kingmed Diagnostics Technology Co., LTD, Guangzhou, People’s Republic of China

3. Guangzhou Women and Children’s Medical Center, Guangzhou, People’s Republic of China

Funder

Science and Technology Plan

Section of Science and Technology

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10245332.2017.1422315

Reference33 articles.

1. Blood coagulation factor XIII and factor XIII deficiency

2. An update of the mutation profile of Factor 13 A and B genes

3. Factor XIII, clot structure, thrombosis

4. Characterization of the gene for the a subunit of human factor XIII (plasma transglutaminase), a blood coagulation factor.

5. Deficiency of Factor XIII Gene in Chinese: 3 Novel Mutations

Cited by 6 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. Novel Insights into Heterozygous Factor XIII Deficiency;Seminars in Thrombosis and Hemostasis;2023-03-20

2. Congenital Factor XIII Deficiency, Diagnosis, and Management;Congenital Bleeding Disorders;2023

3. Noninvasive prenatal diagnosis of congenital factor XIII deficiency in Iran;Blood Coagulation & Fibrinolysis;2022-01-03

4. Prenatal diagnosis of factor 13 deficiency and its recurrence;BMJ Case Reports;2020-12

5. Premarital Screening Program for Congenital Factor XIII Deficiency in Iran;Clinical Laboratory;2020

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