unusual etiology of acute myocardial infarction – factor v leiden mutation
Abstract
Factor V Leiden is the most common cause of inherited thrombophilia in Caucasian populations, accounting for 40-50% of cases. The prothrombin gene mutation, deficiencies in protein S, protein C, and antithrombin account for most of the remaining cases.
Access
Citation
ID:
179161
References
Blockchain Verification
Account:
NFT Contract Address:
0x95644003c57E6F55A65596E3D9Eac6813e3566dA
Article ID:
179161
Unique Identifier:
https://doi.org/10.17987/icfj.v4i0.126
Network:
Scimatic Chain (ID: 481)
Loading...
Blockchain Readiness Checklist
Authors
Abstract
Journal Name
Year
Title
Creates 1,000,000 NFT tokens for this article
Token Features:
- ERC-1155 Standard NFT
- 1 Million Supply per Article
- Transferable via MetaMask
- Permanent Blockchain Record
Scan with Saymatik Web3.0 Wallet
