Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review-Reference-Cited by-同舟云学术

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Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review

Published:2022-10-21 Issue:42 Volume:101 Page:e31221
ISSN:1536-5964
Container-title:Medicine
language:en
Short-container-title:

Author:

Zhang Zhaorui,Yang Zhen,Chen Mei,Li Yuzhu

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference33 articles.

1. Current management of acute pulmonary embolism.;Martinez Licha;Ann Thorac Cardiovasc Surg,2020

2. Interventional therapies in acute pulmonary embolism.;Zhang;Interv Cardiol Clin,2020

3. Venous thromboembolism in Asia – an unrecognised and under-treated problem.;Angchaisuksiri;Thromb Haemost,2011

4. PC deficiency testing: thrombin-thrombomodulin as PC activator and aptamer-based enzyme capturing increase diagnostic accuracy.;Reda;Front Cardiovasc Med,2021

5. The phenotypic and genetic assessment of protein C deficiency.;Cooper;Int J Lab Hematol,2012

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