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1 ensaios clínicos encontrados.
[Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene].
Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation.
An unanticipated prolonged baseline ACT during cardiac surgery due to factor XII deficiency.
🥈 ObservacionalCongenital hemophilia A with low activity of factor XII: a case report and literature review.
🥈 Ensaio clínicoThe Standard Point-of-Care Hemochron Jr. ACT+ Test in Monitoring Heparin Administration for Cardiopulmonary Bypass in Severe Factor XII Deficiency.