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Clinical and functional characterization of a novel heterozygous mutation c.473T > A (p.Leu158Gln) in the SERPINC1 gene causing recurrent arteriovenous thrombophilia

Crossref DOI link: https://doi.org/10.1186/s12959-025-00801-0

Published Online: 2025-11-20

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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