A novel plasminogen mutation in a child with hereditary periodic syndrome: A case report-Reference-Cited by-同舟云学术

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A novel plasminogen mutation in a child with hereditary periodic syndrome: A case report

Published:2022-04-20 Issue:4 Volume:2 Page:237-243
ISSN:2767-1429
Container-title:Rheumatology & Autoimmunity
language:en
Short-container-title:Rheumatology & Autoimmunity

Author:

Akbar Lujayn¹,Alazami Anas M.²,AlSaleem Alhanouf¹,Alsonbul Abdullah¹,Al‐Mayouf Sulaiman M.¹³^ORCID

Affiliation:

1. Pediatric Rheumatology King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

2. Translational Genomics, Centre for Genomic Medicine King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

3. College of Medicine Alfaisal University Riyadh Saudi Arabia

Publisher

Wiley

Subject

Rheumatology,Internal Medicine,Immunology and Allergy,Immunology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rai2.12036

Reference23 articles.

1. Current and future advances in genetic testing in systemic autoinflammatory diseases

2. Autoinflammatory diseases in childhood;Yıldız M;Balkan Med J,2020

3. A critical role for plasminogen in inflammation

4. The multifaceted role of plasminogen in inflammation

5. Ligneous periodontitis in a patient with type 1 plasminogen deficiency: a case report and review of the literature;Sadasivan A;Case Rep Dent,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. Plasminogen missense variants and their involvement in cardiovascular and inflammatory disease;Frontiers in Cardiovascular Medicine;2024-06-25

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