The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascade

Eitemau Tebyg

• Molecular Basis of the Clotting Defect in a Bleeding Patient Missing the Asp-185 Codon in the Factor X Gene
  gan: Lu, Qiuya, et al.
  Cyhoeddwyd: (2014)
• Protein C Thr315Ala variant results in gain of function but manifests as type II deficiency in diagnostic assays
  gan: Ding, Qiulan, et al.
  Cyhoeddwyd: (2015)
• Paradoxical bleeding and thrombotic episodes of dysprothrombinemia due to a homozygous Arg382His mutation
  gan: Ding, Qiulan, et al.
  Cyhoeddwyd: (2016)
• Gly74Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant function
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  Cyhoeddwyd: (2017)
• Thr90Ser mutation in antithrombin is associated with recurrent thrombosis in a heterozygous carrier
  gan: Lu, Yeling, et al.
  Cyhoeddwyd: (2020)