Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference25 articles.
1. The protein C anticoagulant system: inherited defects as basis for venous thrombosis;Dahlback;Thromb Res,1995
2. Progress in the understanding of the protein C anticoagulant pathway;Dahlback;Int J Hematol,2004
3. The nucleotide sequence of the gene for human protein C;Foster;Proc Natl Acad Sci USA,1985
4. Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH;Reitsma;Thromb Haemost,1995
5. Inherited thrombophilia: Part 1;Lane;Thromb Haemost,1996
Cited by 5 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. Molecular and clinical characterization of two independent Chinese families with protein C deficiency;2024-06-04
2. Digenic Inheritance of PROC and SERPINC1 Mutations Contributes to Multiple Sites Venous Thrombosis;Hämostaseologie;2024-01-15
3. Prevalence, Genetic Background, and Clinical Phenotype of Congenital Thrombophilia in Chronic Thromboembolic Pulmonary Hypertension;JACC: Asia;2022-06
4. Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families;Blood Coagulation & Fibrinolysis;2021-07-13
5. A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families;Blood Coagulation & Fibrinolysis;2016-10
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3