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Three novel ATG16L1 mutations in a patient with acute myocardial infarction and coronary artery ectasia: A case report
INTRODUCTION: Acute myocardial infarction (AMI) is a specific type of coronary artery disease (CAD) caused by the rupture of coronary atherosclerotic plaques. Coronary artery ectasia (CAE) is a rare phenotype of cardiovascular disease that may promote thrombosis and inflammatory responses leading to...
Tallennettuna:
| Julkaisussa: | Medicine (Baltimore) |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Lippincott Williams & Wilkins
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7850772/ https://ncbi.nlm.nih.gov/pubmed/33530273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000024497 |
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