Abstract
A genetic variation in the 3'-UT region of the prothrombin gene, a G to A mutation at nucleotide 20210, has been associated recently with increased risk of acute myocardial infarction. We describe a case of a young patient carrying the mutation, with an AMI caused by large bilateral intracoronary thrombi, that underwent direct PTCA
| Original language | English |
|---|---|
| Pages (from-to) | 427-430 |
| Journal | Catheterization and cardiovascular diagnosis |
| Volume | 44 |
| Issue number | 4 |
| Publication status | Published - 1998 |
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SDG 3 Good Health and Well-being
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