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ArticleThrombosis journal2025

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

Zhong Chongxia et al.PubMed ↗Full text ↗Publisher ↗

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2025
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Full record →Abstract, authors, funding and every citing paper · PMID 41267092